Bennett Greenspan: Meet My Extended Family & Discover Extraordinary Deep Heritage

“My ancestors are in my soul. I can’t get them out of my mind.”

Bennett Greenspan

“And yes, I brake for cemeteries.”

Bennett Greenspan gave an incredibly interesting presentation at the 15th International Genetic Genealogy Conference held by FamilyTreeDNA in November 2023. Since his retirement in January 2021, he has been able to focus on his genealogy. Once a genealogist, always a genealogist.

Bennett said some things I hadn’t thought about, and now I’m viewing Y-DNA matches with a different perspective – based on how he’s using his results.

Ever since I met him, Bennett’s focus has been to use genetics to unravel his complex Jewish heritage.

The questions that drive Bennett are the same ones that motivate most genealogists:

  1. Who are we?
  2. Where did we come from?
  3. Where were we before we were there?
  4. How did my ancestors get there?

Bennett “lost his family lines” before the mid-1800s due to his Jewish heritage, exacerbated in the 1930s by the devastation wrought by the Holocaust. Families were either killed or scattered to survive. It has been through Y-DNA in particular that he has been able to establish unquestionable and confirmed connections with other Greenspan men, sometimes by similar but different surnames, like Green, and sometimes with other surnames entirely.

When Bennett first started down this path, he tested more than 62 men before actually finding one a decade later that matched his Y-DNA. Bennet commented that it was “a little frustrating.”

Persistence is the key, and sometimes, genealogy is a waiting game, but that’s small comfort to genealogists during that unproductive waiting period.

Eventually, Bennett reassembled his family, at least somewhat, but it was a long journey. Here’s Bennett’s incredible story, including surprises, as he tells it.

Bennett discovered genealogy at age 12 and, like many genealogists, created a pedigree chart by talking to his family.

I love the mark-outs. How many of us still have our first chart with its edits?

This is the young Bennett Greenspan, whose interest in genealogy would one day unlock secrets for all of us!

It was a long way from a decade with no matches to finding his genetic kin in Ukraine.

The Big Y-700 Time Tree shows Bennett’s lineage in Ukraine, but stepping back in time, some descendants of his ancestors are found in adjacent locations.

Bennett was passionately discussing his matches on the time tree and in the Greenspan project, so I visited the Greenspan DNA Project, where the earliest known ancestors of Bennett’s Big Y matches are shown on the Group Time Tree.

Bennett’s closest matches are shown as descendants of haplogroup J-ZS1718. He has additional matches who are not in the Greenspan project. Since this is the Group Time Tree, it only displays the people in that project, along with their earliest known ancestors, Isaac and Usher Greenspan.

12-Marker Matches

Bennett never fails to amaze me. He said something very important and profound about 12-marker matches that I really hadn’t thought about – at least not this way.

As a community, we are often guilty of discounting 12-marker matches, those that don’t match us at 25-markers or above, or with different surnames, as “too far back in time” or otherwise irrelevant. I always look at the names and earliest known ancestors of 12-marker matches, because that person may have tested back in the day when fewer markers were available. But if I don’t recognize something, I move on.

However, Bennett said that, ”Y-12 matches reach back to a common ancestor. 12-marker matches are not a quirk. They are related to you, just further back in time. You share a common ancestor with them, someplace. They may be more distant, but they are still your close matches.”

I’ve been in too much of a hurry for a quick win, and ignoring the (apparently not so) obvious.

Determining when and where their ancestors lived also paves the way to discover yours. Your Y-DNA and theirs were in the same place at the same time.

Of Bennett’s 171 12-marker matches, 107 have upgraded to the Big Y, probably mostly due to his encouragement. This benefits both them and Bennett by fleshing out the history of that entire group of men, including how they got to where they are found in the first available records. The Time Tree shows when Big Y testers shared a common ancestor, and based on Earliest Known Ancestor (EKA) locations, where. This provides further information about the lives of ancestors before contemporary records – in other words – people that we can never identify by name. It’s a window into ancestors before surnames.

Bennett notes that testers need to know their ancestral village or location to be most useful within the project, and of course, they need to enter their EKA information. Location information is how the Migration Map, Matches Map, and Discover tools, including the Time Tree, are built.

What Happened in Spain?

Bennett’s ancestors and those of his 12-marker matches are found in Spain, and as Bennett says, “One son stayed and one left about the year 296.”

While we have no idea of their names, based on the Time Tree combined with the cluster of earliest known ancestors, we know that they were in Spain, and when.

Their family story is revealed in the bifurcation of the tree found beneath haplogroup J-L823, formed about 296 CE. One line stayed in Spain, and Bennett’s line migrated to eastern Europe where that man’s descendants, including Bennett’s family, are found in the Russian Federation, Belarus, Poland, Lithuania, Sweden, Slovakia, Ukraine, Germany, Romania, the Czech Republic, and other eastern European locations. The closer to you in the tree and in time, the more relevant to your more recent ancestral story.

However, Bennett’s deeper ancestry, the migration of his ancestors to Spain, was only revealed by testing those more distantly related men. Those same men could well have been ignored entirely because they only matched at 12 markers.

According to Bennett, “Y-12 markers are important because these are the men most closely related to you in a database of 1 million men.”

How incredibly profound. How much have I been cavalierly overlooking?

How does this actually apply to Bennett’s results?

Bennett’s Spanish Matches

Bennett has the following STR panel matches who indicate that their EKA are from Spain. You can see that they match Bennett on a variety of panels.

  • X = yes, match
  • No = no match
  • Blank = not tested at that level.

In the Big Y GD column, the genetic distance (GD) is displayed as 15/660 where 15 is the number of mismatches, or the cumulative genetic distance ABOVE the 111 panel, and 660 is the number of STR markers above 111 with results.

The Big Y-500 test guaranteed a minimum of 500 total STR markers, and the Big Y-700 guarantees a minimum of 700 total STR markers, plus multiple scans of the balance of the Y chromosome for SNP mutations that define haplogroups. Testers don’t receive the same number of markers because the scan technology sometimes doesn’t read a specific location.

Tester 12 25 37 67 111 Big Y Test Big Y GD Big Y Match Haplogroup
AA X X X No No Yes 15/660 No J-FTD8826
DT X X No No X Yes 17/664 No J-FTE50318
JG X X No No
AR No No X X No No
ELR X X X No No
EL X X Yes 17/666 No J-FTE50318
GC X X X X No No
JC X No No
JLG X X No No No Yes 14/662 No J-FTE23540
MF X X No X No Yes 15/665 No J-FTD91126
MT X X X X No No
BE X X X X X Yes 20/664 No J-BY1795
DR X X X X X Yes 16/660 No J-FTC87344
EC X X X X X Yes 15/665 No J-FTC87344
GM X X No No No Yes 16/650 No J-FTD28153
GM X X X X No Yes 17/664 No J-FTD11019
LS X X No No No Yes 18/666 No J-FTD28153
NE X X X X X Yes 23/597 No J-BY1795
NC X No No
RR X X X No X Yes 22/659 No J-BY1795
TT X X X X X Yes 16/647 No J-FTC87344
XG X X X No No Yes 17/523 No J-BY167283
JA X X No No No Yes 15/646 No J-FTD11019

Of those 23 Spanish matches, sixteen have upgraded to Big Y tests, 14 of which are Big Y-700s, resulting in nine different haplogroups, all of which are descendants of Haplogroup J-L823. How cool is that?

The “Nos” in the Big Y Match Column aren’t mistakes. That’s right – none of these men match Bennett on the Big Y test, meaning they had more than a 30 mutation difference between them and Bennett on the Big Y test.

At first glance, you’d think that Bennett would have been disappointed, but that’s not the case at all! In fact, it was the information provided by these distant Spanish matches that provided Bennett with the information that his line had split sometime around the year 296 CE, with one branch remaining in Spain and his branch migrating to Eastern Europe, where he has lots of matches.

DNA Plus History

What was happening in Spain or the Iberian peninsula that involved the Jewish people about that time? Historical records exist of Jews living in that region before the fall of the Second Temple in about 70 CE, including records of Jews being expelled from Rome in 139 for their “corrupting influence.”

Furthermore, the Ancient DNA Connections for haplogroup J-L823, the most recent common ancestor (MRCA) for all of those branches, includes connections to multiple burials from:

  • Lebanon
  • Iran
  • Rome (from 1-400 CE)
  • Turkey
  • Jordan

Clearly, Bennett’s ancestor was in the Iberian peninsula around or before 296 CE. One branch stayed, winding up in Spain, and one headed for Europe.

Without these matches, some who didn’t match above the 12 or 25 marker level, how would Bennett have EVER known that his Jewish ancestors left the Middle East for Spain in the early years? How would he have known they migrated from Spain to Eastern Europe, and how would he have known that his line did not migrate directly from the Levant to Eastern Europe in the 9th century?

Big Y matches are typically within about 1500 years, but non-matches are still INCREDIBLY valuable. Without them, you can’t completely assemble your family story.

I noticed on the Time Tree that in Bennett’s Eastern European line, one of his ancestor’s brother lineages includes the Katzenellenbogen Rabbinic Lineage derived from ancient DNA samples.

Bennett’s successes have resulted from contacting his matches and encouraging upgrades. So how did he do it? What’s the magic sauce?

Contacting Matches

How to contact matches successfully is a question I see often. In fact, FamilyTreeDNA recently wrote about that in an article, here.

Bennett’s methodology for contacting his matches to encourage an upgrade is that he sends an email explaining why he’s encouraging them to upgrade, followed by a 2nd email three days later.

Bennett tells the recipient that we are at an inflection point in time. “It’s winter, the wind is blowing hard, and many of the leaves are gone.”

In other words, we need to cast the net wider and capture what we can, while we can. Unfortunately, many early testers have died, and with them, chapters of history are perishing.

Collaboration is key. In addition to encouraging upgrades, Bennett also offers Zoom calls to these groups of men to explain the results if they are interested.

What a GREAT idea! I need to begin offering that as well.

Upgrade Request

Bennett reaches out to his matches at various levels, but he expects his closer STR matches, meaning at the 67 and 111 marker level with the fewest mismatches, to match him on a Big Y-700 test and connect someplace between 300-600 years ago, which helps everyone flesh out their tree.

Bennett’s email:

Hello <name>,

Since you have already made a sizable investment in your Y-DNA, you now know that we come from the dominant male Middle Eastern group (Haplogroup J) of men who <subject here>.

What’s really neat is that our Y-DNA has recently been found in an archaeological site in Northwestern Jordan dated to about 4200 years ago. I know this because I upgraded to the Big Y, which tests SNPs, looking at several million locations on the Y chromosome of each man.

One academic customer recently compared this new technology as the difference between looking into space with binoculars versus the Hubble Telescope.

I don’t know if you are familiar with your list of matches at the highest level you’ve tested for, either Y-67 or Y-111. If you are, you should recognize my name and the names of others who have taken the Big Y test.

You’ll see what you’ll gain by letting me upgrade your test for you and determining whether you are related to my line – probably between about 200 years and 500 years.

This might be the second time that I have written to you on this matter; can I presume if I don’t hear from you that you’re not really interested in the Y-DNA subject anymore?

Can I run the test so that I can see how closely we are related – at my expense? (Of course, you get to see how closely related we are, too).

Please reply to me and say “yes.” You don’t even have to put a 🙂 if you don’t want to.

I started this company and this industry over 20 years ago. I predict that you will be happy with the history of YOU that this upgrade will uncover.

Best,

Bennett Greenspan

As you can see, this email can easily be personalized further and adapted to matches at the 37, 25, and 12 marker levels – or even Family Finder matches, now that intermediate-range haplogroups are being reported.

What’s Next?

I’m going back to every one of the kits I sponsored or that represent descendants of one of my ancestors to review their matches again – focusing not just on the closest matches with common surnames, but also on locations – and specifically at lower matching levels. I’ll also be checking their Family Finder matches for male surname matches, or similar surnames.

As is evident from Bennett’s tests, an entire mine of diamonds is out there, just waiting to be unearthed by a Big Y test.

And to think that some people have been advising people to ignore 12-marker matches out-of-hand because they are “entirely irrelevant.” They aren’t – for two reasons.

  1. First, some early testers only tested to that level
  2. Second, because of the deeper history that Big Y tests from those matches will uncover

You can view your Y-DNA matches, upgrade your own Y-DNA test, or order a Big Y-700 test if you haven’t yet tested by clicking here. What’s your next step?

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FamilyTreeDNA 2023 Update – Past, Present and Future

At the FamilyTreeDNA International Conference on Genetic Genealogy, held November 3-5 in Houston for group project administrators, product and feature updates were scattered across both days in various presentations.

I’ve combined the updates from FamilyTreeDNA into one article.

I’ve already written two articles that pertain to the conference.

FamilyTreeDNA has already begun rolling the new Y DNA haplogroups from Family Finder autosomal tests, which I wrote about here:

I still have at least two more articles to publish from this conference that was chocked full of wonderful information from a wide range of talented speakers.

Past, Present, and Future with Katy Rowe-Schurwanz

Katy Rowe-Schurwanz, FamilyTreeDNA’s Product Manager, provided an update on what has been accomplished in the four and a half years since the last conference, what’s underway now, and her wish list for 2024.

Please note the word “wish list.” Wish list items are NOT commitments.

Recent Milestones

A lot has been happening at FamilyTreeDNA since the last conference.

Acquisition and Wellness Bundles

As everyone is aware, at the end of 2020, myDNA acquired Gene by Gene, the parent company of FamilyTreeDNA, which included the lab. As a result, the FamilyTreeDNA product menu has expanded, and wellness bundles are now available for FamilyTreeDNA customers.

If you’re interested, you can order the Wellness product in a bundle with a Family Finder test, here.

You can add the Wellness product for $39 if you’ve already tested.

New TIP (Time Prediction) STR Report

Did you notice that the old TIP report for Y DNA STR markers was replaced with an updated version several months ago?

To view the new report, sign on and select your Y DNA matches. At the far right of each match you’ll see these three icons representing a pedigree chart, notes, and the TIP (Time Predictor) report.

The updated TIP report includes wonderful new graphs and age estimates for each match category, which you can read about, here. Each category, such as 67-marker matches, has time estimates in which a common ancestor might have lived at each possible genetic distance.

Math is our friend, and thankfully, someone else has done it for us!

Please note that the Big Y SNP dates are MUCH more accurate for a variety of reasons, not limited to the instability and rapid mutation rate of STR mutations.

MyOrigins3

MyOrigins3, FamilyTreeDNA’s ethnicity offering, added over 60 new reference populations for a total of 90, plus chromosome painting. You can read about MyOrigins features here, and the white paper, here.

This is one of my favorite improvements because it allows me to identify the segment location of my population ancestries, which in turn allows me to identify people who share my minority segments such as Native American and African.

Due to a lack of records, these relationships are often exceedingly difficult to identify, and MyOrigins3 helps immensely.

Additional Releases

Additional products and features released since the last conference include:

Discover

Released in July 2022, Discover is the amazing new free product that details your ancestor’s Y DNA “story” and his walk through time and across the globe.

In the past 18 months, all of the Discover features are new, so I’m only making a brief list here. The great thing is that everyone can use Discover if you know or can discover (pardon the pun) the haplogroup of your ancestral lines. Surname projects are often beneficial for finding your lineages.

  • Haplogroup Story includes haplogroup location, ages derived from the earliest known ancestor (EKA) of your matches, and ancient DNA samples. Please be sure you’ve entered or updated your EKA, and that the information is current. You can find instructions for how to update or add your EKA here.
  • A recent addition to the haplogroup story includes Haplogroup Badges.
  • Country Frequency showing where this haplogroup is found with either a table view or an interactive map
  • Famous and infamous Notable Connections, including Mayflower passengers, Patriots from the American Revolution, US presidents, royal houses, artists, musicians, authors, pirates, sports figures, scientists, and more.

If you know of a proven connection to a notable figure, contact customer support and let them know! Notable connections are added every week.

One famous Discover connection is Ludwig von Beethoven which resulted from a joint academic study between FamilyTreeDNA and academic researchers. It’s quite a story and includes both a mystery and misattributed parentage. You can see if you match on Discover and read about the study, here.

  • Updated Migration Map, including locations of select ancient DNA sites
  • The Time Tree, probably the most popular Discover report, shows the most current version of the Y DNA phylotree, updated weekly, plus scientifically calculated ages for each branch. Tree node locations are determined by your matches and their EKA countries of origin. I wrote about the Time Tree, here.
  • Anticipated in early 2024, the EKA and block tree matches will also be shown on the Time Tree in Discover for individual Big Y testers, meaning they will need to sign in through their kits.
  • The Group Time Tree, visible through group projects, takes the Time Tree a step further by including the names of the EKA of each person on the Time Tree within a specific project. Information is only displayed for project members who have given permission to include their data. You can select specific project groupings to view, or the entire project. I wrote about the Group Time Tree here and here.
  • Globetrekker is an exclusive Big Y mapping feature discussed here, here, here, and here.
  • Ancient Connections includes more than 6,100 ancient Y DNA results from across the globe, which have been individually analyzed and added for matching in Discover. Ancient Connections serve to anchor haplogroups and provide important clues about matches, migration paths and culture. New connections are added weekly or as academic papers with adequate Y DNA coverage are released.
  • Your Ancestral Path, which lists the haplogroups through every step from the tester back to Y Adam and beyond. Additional information for each haplogroup in your path includes “Time Passed” between haplogroups, and “Immediate Descendants,” meaning haplogroups that descend from each subclade. New columns recently added include “Tested Modern Descendants” and “Ancient Connections.”
  • Suggested Projects include surname, haplogroup, and geographic projects. Katy said that people joining projects are more likely to collaborate and upgrade their tests. You can also see which projects other men with this haplogroup have joined, which may well be projects you want to join too.
  • Scientific Details provides additional information, such as each branch’s confidence intervals and equivalent variables (SNPs). You can read more here.
  • Compare Haplogroups is the most recent new feature, added just last month, which allows you to enter any two haplogroups and compare them to determine their most recent common ancestral haplogroup. You can read about Compare Haplogroups, here.

Please note that the Studies feature is coming soon, providing information about studies whose data has been included in Discover.

You can read about Discover here, here, here, and here.

If you’re interested, FamilyTreeDNA has released a one-minute introduction to Y DNA and Discover that would interest new testers, here.

Earliest Known Ancestor (EKA) Improvement

Another improvement is that the earliest known ancestor is MUCH easier to enter now, and the process has been simplified. The EKAs are critical for Discover, so PLEASE be sure you’ve entered and updated your EKA.

Under the dropdown beside your name in the upper right-hand corner of your personal page, select Account Settings, then Genealogy and Earliest Known Ancestors. Complete the information, then click on “Update Location” to find or enter the location on a map to record the coordinates.

It’s easy. Just type or drop a pin and “Save.”

Saving will take you back to the original EKA page. Save that page, too.

Recommended Projects on Haplogroups & SNPs Page

You’re probably aware that Discover suggests projects for Y DNA testers to join, but recommended haplogroup projects are available on each tester’s pages, under the Y DNA Haplotree & SNPs page, in the Y DNA STR results section.

If there isn’t a project for your immediate haplogroup, just scroll up to find the closest upstream project. You can also view this page by Variants, Surnames and Countries.

This is a super easy tool to use to view which surnames are clustered with and upstream of your haplogroup. With Family Finder haplogroups being assigned now, I check my upstream haplogroups almost daily to see what has been added.

For example, my Big Y Estes results are ten branches below R-DF49, but several men, including Estes testers, have been assigned at this level, thanks to Y DNA haplogroups from Family Finder testing. I can now look for these haplogroups in the STR and Family Finder matches lists and see if those men are receptive to Big Y testing.

Abandoned Projects

Sometimes group project administrators can no longer function in that capacity, resulting in the project becoming abandoned. FamilyTreeDNA has implemented a feature to help remedy that situation.

If you discover an abandoned project, you can adopt the project, spruce things up, and select the new project settings. Furthermore, administrators can choose to display this message to recruit co-administrators. I need to do this for several projects where I have no co-admin.

If you are looking for help with your project, you can choose to display the button
through the Project Profile page in GAP. For non-project administrators, if you’d like to help, please email the current project administrators.

New Kit Manager Feature

FamilyTreeDNA has added a “Kit Manager” feature so that an individual can designate another person as the manager of their kit.

This new setting provides an avenue for you to designate someone else as the manager of your DNA test. This alerts FamilyTreeDNA that they can share information with both of you – essentially treating your designated kit manager the same as you.

If you’re the kit manager for someone else, you NEED to be sure this is completed. If that person is unavailable for some reason, and support needs to verify that you have legitimate access to this kit, this form and the Beneficiary form are the ONLY ways they can do that.

If your family member has simply given you their kit number and password, and for some reason, a password reset is required, and their email address is the primary contact – you may be shut out of this kit if you don’t complete this form.

Beneficiary Page

Additionally, everyone needs to be sure to complete the Beneficiary page so that in the event of your demise, FamilyTreeDNA knows who you’ve designated to access and manage your DNA account in perpetuity. If you’ve inherited a kit, you need to add a beneficiary to take over in the event of your death as well.

What is FamilyTreeDNA working on now?

Currently in the Works

Katy moved on to what’s currently underway.

Privacy and Security

Clearly, the unauthorized customer data exposure breach at 23andMe has reverberated through the entire online community, not just genetic genealogy. You can read about the incident here, here, here, and here.

FamilyTreeDNA has already taken several steps, and others are in development and will be released shortly.

Clearly, in this fast-moving situation, everything is subject to change.

Here’s what has happened and is currently planned as of today:

  • Group Project Administrators will be required to reset their password soon.

Why is this necessary?

Unauthorized access was gained to 23andMe accounts by people using the same password for multiple accounts, combined with their email as their user ID. Many people use the same password for every account so that they can remember it. That means that all a hacker needs to do is breach one account, and they can use that same information to “legitimately” sign in to other accounts. There is no way for the vendor to recognize this as unauthorized since they have both your user ID and password.

That’s exactly what happened at 23andMe. In other breaches, this information was exposed, and hackers simply tried the same username and password combination at 23andMe, exposing the entire account of the person whose account they signed in “as.” This includes all of their matches, genetic tree, shared matches, matches of matches, ethnicity, and segments. They could also have downloaded both the match list and the raw DNA file of the compromised account.

At FamilyTreeDNA, project administrators can select their own username, which could be their email, so they will be required to reset their password.

Additional precautions have been put in place on an interim basis:

  • A pause in the ability to download match and segment information.
  • A pause in accepting 23andMe uploads.

Administrators will also be required to use two-factor authentication (2FA.) To date, two of the four major vendors are requiring 2FA. I would not be surprised to see it more broadly. Facebook recently required me to implement 2FA there, too, due to the “reach” of my postings, but 2FA is not required of everyone on Facebook.

Please note that if you received an email or message that is supposedly from any vendor requiring 2FA, GO DIRECTLY TO THAT VENDOR SITE AND SIGN IN.  Never click on a link in an email you weren’t expecting. Bad actors exploit everything.

Customers who are not signing in as administrators are not required to implement 2FA, nor will they be required to reset their password.

Personally, I will implement 2FA as soon as it’s available.

While 2FA is an extra step, it’s easy to get used to, and it has already literally saved one of my friends from an authorized hack on their primary and backup email accounts this week. Another friend just lost their entire account on Facebook because someone signed in as them. Their account was gone within 15 minutes.

2FA is one of those things you don’t appreciate (at all) until it saves you, and then, suddenly, you’re incredibly grateful.

At this point in time, FamilyTreeDNA users will NOT be required to do a password reset or implement 2FA. This is because customers use a kit number for sign-in and not a username or email address. I would strongly recommend changing your password to something “not easy.” Never reuse passwords between accounts.

I really, really want you to visit this link at TechRepublic and scroll down to Figure A, which shows how long it takes a hacker to crack your password. I guarantee you, it’s MUCH quicker than you’d ever expect.

Kim Komando wrote about this topic two years ago, so compare the two charts to see how much easier this has become in just two years.

Again, if you receive an email about resetting your password, don’t click on a link. Sign in independently to the vendor’s system, but DO reset your password.

FamilyTreeDNA also engages in additional security efforts, such as ongoing penetration testing.

New Permissions

Additionally, at FamilyTreeDNA, changes were already in the works to separate out at least two permissions that testers can opt-in to without granting project administrators Advanced rights.

  • Download data
  • Purchase tests

The ability to purchase tests can be very important because it allows administrators to order and pay for tests or upgrades on behalf of this tester anytime in the future.

Family Finder Haplogroups

FamilyTreeDNA has already begun releasing mid-level Y DNA haplogroups for autosomal testers in a staggered rollout of several thousand a day.

I wrote about this in the article, FamilyTreeDNA Provides Y DNA Haplogroups from Family Finder Autosomal Tests, so I’m not repeating all of that information here – just highlights.

  • The Family Finder haplogroup rollout is being staggered and began with customers on the most recent version of the testing chip, which was implemented in March of 2019.
  • Last will be transfers/uploads from third parties.
  • Haplogroups resulting from tests performed in the FTDNA labs will be visible to matches and within projects. They will also be used in both Discover and the haplotree statistics. This includes Family Finder plus MyHeritage and Vitagene uploads.
  • Both MyHeritage and Vitagene are uploaded or “transferred” via an intracompany secure link, meaning FamilyTreeDNA knows that their information is credible and has not been manipulated.
  • Haplogroups derived from tests performed elsewhere will only be visible to the user or a group administrator viewing a kit within a project. They will not be visible to matches or used in trees or for statistics.
  • Any man who has taken a Y DNA STR test will receive a SNP-confirmed, updated haplogroup from their Family Finder test that replaces their predicted haplogroup from the STR test.

Please read this article for more information.

New Discover Tools and Updates

Discover content continues to be updated, and new features are added regularly, creating an increasingly robust user experience.

Soon, group administrators will be able to view all Discover features (like Globetrekker) when viewing kits of project members who have granted an appropriate level of access.

Ancient and Notable connects are added weekly, and a new feature, Study Connections, will be added shortly.

Study Connections is a feature requested by customers that will show you which study your academic matches came from. Today, those results are used in the Y DNA tree, but the source is not detailed.

Anticipated in early 2024, the EKA and block tree matches will also be shown on the Time Tree in Discover for individual Big Y testers (not publicly).

Big Y FaceBook Group

FamilyTreeDNA has ramped up its social media presence. They launched the Big Y Facebook group in July 2023, here, which currently has just under 9000 members. Several project administrators have volunteered their time to help manage the group.

FamilyTreeDNA Blog

In addition, FamilyTreeDNA is publishing at least one blog article each week, and sometimes more. You can view or subscribe here. Some articles are written by FamilyTreeDNA staff, but project administrators and customers author other content.

Multi-Language Support

Translation of the main FamilyTreeDNA website and results pages to Spanish has begun, with more languages planned soon.

Paypal, Payments, and Gift Cards

Paypal has been added as a payment selection, along with a PayPal option that provides the ability to make payments.

Additionally, a gift card can be purchased from the main page.

Million Mito Project & Mitotree

Work on the Million Mito Project is ongoing.

The Million Mito Project was launched in 2020 as a collaborative effort between FamilyTreeDNA’s Research & Development Team and the scientific portion of the Genographic Project. I’m a team member and wrote about the Million Mito Project, here.

We’re picking up from where the Phylotree left off in 2016, analyzing 20 times more mtDNA full sequences and reimagining the mtDNA Haplotree. By examining more mtDNA data and applying the processes that allowed FamilyTreeDNA to build the world’s largest Y DNA Haplotree, we can also create the world’s largest Mitotree.

In 2022, the first update was released, authored by the Million Mito team, with the discovery of haplogroup L7. You can read about this amazing discovery rooted deep in the tree here, here, and here. (Full disclosure: I’m a co-author.)

Not only that, but “Nature Scientific Reports” selected this article as one of five named Editor’s Choice in the Mitogenomics category, here. In the science world, that’s a HUGE deal – like the genetic Emmy.

Here’s one example of the type of improvements that can be expected. Currently, the formation of haplogroup U5a2b2a reaches back to about 5000 years ago, but after reanalysis, current branches originated between 500 and 2,500 years ago, and testers are clustered more closely together.

This is SOOO exciting!!!

Just as Discover for Y DNA results was built one feature at a time, the same will be true for MitoDiscover. That’s my name, not theirs.

As the new Mitotree is rolled out, the user interface will also be updated, and matching will function somewhat differently. Specifically, it’s expected that many more haplogroups will be named, so today’s matching that requires an exact haplogroup match to be a full sequence match will no longer work. That and other matching adjustments will need to be made.

I can hardly wait. I have so many results I need to be able to view in a tree format and to place in a timeframe.

You can be included in this exciting project, learn more about your matrilineal (mother’s) line, and hopefully break down some of those brick walls by taking the full sequence mitochondrial DNA test, here.

After the new Mitotree is rolled out and the Y DNA Family Finder haplogroups are completed, Family Finder customers, where possible, will also receive at least a basic-level mitochondrial haplogroup. Not all upload files from other vendors include mtDNA SNPs in their autosomal files. The mitochondrial Family Finder haplogroup feature isn’t expected until sometime in 2025, after the new tree and MitoDiscover are complete.

The Future

What’s coming later in 2024, or is ongoing?

Privacy Laws

Most people aren’t aware of the new privacy laws in various states, each of which has to be evaluated and complied with.

The effects of these changes will be felt in various areas as they are implemented.

New Kits Opted Out of IGG

Since late August, all new FTDNA kits are automatically opted OUT of Investigative Genetic Genealogy (IGG) by default.

Regular matching consent and IGG matching consent have been separated during onboarding.

Biobanking Separate Consent

Another consent change is to have your sample biobanked. FamilyTreeDNA has always maintained your sample for “roughly 25 years.” You could always ask to have your sample destroyed, but going forward, you will be asked initially if you want your sample to be retained (biobanked.) It’s still free.

Remember, if someone declines the biobanking option, their DNA will be disposed of after testing. They can’t order upgrades without submitting a new sample. Neither can their family after they’re gone. I ordered my mother’s Family Finder test many years after she had gone on to meet our ancestors – and I’m incredibly grateful every single day.

MyHeritage Tree Integration

An exciting change coming next year is tree integration with MyHeritage.

And no, before any rumors get started, FAMILYTREEDNA IS NOT MERGING WITH MYHERITAGE. It’s a beneficial marriage of convenience for both parties.

In essence, one of the primary focuses of MyHeritage is trees, and they do that very well. FamilyTreeDNA is focused on DNA testing and their existing trees have had issues for years. MyHeritage trees are excellent, support pedigree collapse, provide search capabilities that are NOT case sensitive, SmartMatching, and much more.

If you don’t have a MyHeritage account, creating one is free, and you will be able to either port your existing FamilyTreeDNA tree, or begin one there. If you’re already a MyHeritage member, FamilyTreeDNA and MyHeritage are planning together for a smooth integration for you. More detailed information will be forthcoming as the integration progressed and is released to customers.

You’ll be able to connect multiple kits to your tree at MyHeritage, just like you can at FamilyTreeDNA today, which enables family matching, aka bucketing.

You can also have an unlimited number of different trees at MyHeritage on the same account. You’re not limited to one.

After you link your initial FamilyTreeDNA kit to the proper person in your MyHeritage tree, you’ll be able to relink any currently linked kits.

MyHeritage will NOT receive any DNA information or match information from FamilyTreeDNA, and yes, you’ll be able to use the same tree independently at MyHeritage for their DNA matching.

You’ll still be able to view your matches’ trees, except it will actually be the MyHeritage tree that will be opened at FamilyTreeDNA in a new tab.

To the best of my knowledge, this is a win-win-win, and customers of both companies aren’t losing anything.

One concern is that some FamilyTreeDNA testers have passed away and cannot transition their tree, so a view-only copy of their tree will remain at FamilyTreeDNA so that their matches can still see their tree.

Big Y Infrastructure

Katy mentioned that internal discussions are taking place to see what changes could be made to improve things like matching and test processing times.

No changes are planned for SNP or STR coverage, but discussions are taking place about a potential update to the Telomere to Telomere (T2T) reference. No promises about if or when this might occur. The last part of the human genome to be fully sequenced, the T2T reference model includes the notoriously messy and unreliable region of the Y chromosome with many repeats, duplications, gaps, and deletions. Some data from this region is probably salvageable but has previously been omitted due to the inherent problems.

I’m not sure this shouldn’t be in the next section, the Wishlist.

Wishlist

There are lots of good things on the Wishlist – all of which I’d love.

I’d have difficulty prioritizing, but I’d really appreciate some Family Finder features in addition to the items already discussed. I’d also like to see some GAP (administrator) tool updates.

Which items do you want to see most?

Katy said that FamilyTreeDNA is NOT planning to offer a Whole Genome Sequencing (WGS) test anytime soon. So, if you’re holding your breath, please don’t. Based on what Katy did say, WGS is very clearly not a consideration in 2024 and I don’t expect to see it in 2025 either unless something changes drastically in terms of technology AND pricing.

While WGS prices have come down, those consumer tests are NOT scanned at the depth and quality required for advanced tests like the Big Y or even Family Finder. Normally consumer-grade WGS tests are scanned between 2 and 10 times, where the FamilyTreeDNA lab scans up to 30 times in order to obtain a quality read. 30X scans are in the same category as medical or clinical grade whole genome scans. Significantly higher quality scans mean significantly higher prices, too, so WGS isn’t ready for genealogy prime time yet.

Additionally, commercially available WGS tests are returned to the customer “as is,” and you’re left to extract the relevant SNPs and arrange them into files, or find someone else to do that. Not to mention, in order to preserve the integrity of their database, FamilyTreeDNA does not accept Y or mitochondrial DNA uploads.

Recently, I saw two WGS files with a 20-25% no-call rate for the autosomal SNPs required for the Family Finder test. Needless to say, that’s completely unacceptable. Some tools attempt to “fix” that mess by filling in the blanks in the format of either a 23andMe or Ancestry file so you can upload to vendors, but that means you’re receiving VERY unreliable matches.

The reason none of the major four vendors offer WGS testing for genealogists is because it’s not financially feasible nor technologically beneficial. The raw data file alone won’t fit on most home computers. WGS is just not soup yet, and it won’t be for the general consuming public, including relevant tools, for at least a few years.

I’ve had my whole genome sequenced, and trust me, I wish it were feasible now, but it just isn’t.

Suggestions Welcomed

Katy said that if you have suggestions for items NOT on the wishlist today to contact her through support.

I would add that if you wish to emphasize any specific feature or need above others, please send that feedback, politely, to support as well.

Katy ended by thanking the various teams and individuals whose joint efforts together produce the products we use and enjoy today.

Lab Update

Normally, DNA testing companies don’t provide lab updates, but this conference is focused on group project administrators, who are often the most dedicated to DNA testing.

A lab update has become a tradition over the years.

Linda Jones, Lab Manager, provided a lab update.

You may or may not know that the FamilyTreeDNA lab shifted gears and stepped up to handle Covid testing.

Supply-chain shortages interfered, but the lab ran 24×7 between 2020 and 2022.

Today, the lab continues to make improvements to processes with the goal of delivering the highest quality results in a timely manner.

On Monday, after the conference, attendees could sign up for a lab tour. You might say we are a rather geeky bunch and really enjoy the science behind the scenes.

Q&A and Thank You

At the end of the conference, the FamilyTreeDNA management team answered questions from attendees.

Left to right, Daniel Au, CTO; Linda Jones, Lab Manager; Katy Rowe-Schurwanz, Product Manager; Clayton Conder, VP Marketing; Goran Runfeldt, Head of R&D; and Andrew Gefre, Development Manager. Not pictured, Jeremy Balkin, Support Manager; Kelly Jenkins, VP of Operations; and Janine Cloud, Group Projects Manager. Janine is also responsible for conferences and events, without whom there would have been no 2023 FamilyTreeDNA conference. Janine, I can’t thank you enough!

A huge thanks to all of these people and many others, including the presenters, CSRs,  IT, and other FamilyTreeDNA team members for their support during the conference, enabling us to enjoy the conference and replenish the well of knowledge.

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The Best of 2022

It’s that time of year where we look both backward and forward.

Thank you for your continued readership! Another year under our belts!

I always find it interesting to review the articles you found most interesting this past year.

In total, I published 97 articles in 2022, of which 56 were directly instructional about genetic genealogy. I say “directly instructional,” because, as you know, the 52 Ancestors series of articles are instructional too, but told through the lives of my ancestors. That leaves 41 articles that were either 52 Ancestors articles, or general in nature.

It has been quite a year.

2022 Highlights

In a way, writing these articles serves as a journal for the genetic genealogy community. I never realized that until I began scanning titles a year at a time.

Highlights of 2022 include:

Which articles were your favorites that were published in 2022, and why?

Your Favorites

Often, the topics I select for articles are directly related to your comments, questions and suggestions, especially if I haven’t covered the topic previously, or it needs to be featured again. Things change in this industry, often. That’s a good thing!

However, some articles become forever favorites. Current articles don’t have enough time to amass the number of views accumulated over years for articles published earlier, so recently published articles are often NOT found in the all-time favorites list.

Based on views, what are my readers’ favorites and what do they find most useful?

In the chart below, the 2022 ranking is not just the ranking of articles published in 2022, but the ranking of all articles based on 2022 views alone. Not surprisingly, six of the 15 favorite 2022 articles were published in 2022.

The All-Time Ranking is the ranking for those 2022 favorites IF they fell within the top 15 in the forever ranking, over the entire decade+ that this blog has existed.

Drum roll please!!!

Article Title Publication Date 2022 Ranking All-Time Ranking
Concepts – Calculating Ethnicity Percentages January 2017 1 2
Proving Native American Ancestry Using DNA December 2012 2 1
Ancestral DNA Percentages – How Much of Them in in You? June 2017 3 5
AutoKinship at GEDmatch by Genetic Affairs February 2022 4
442 Ancient Viking Skeletons Hold DNA Surprises – Does Your Y or Mitochondrial DNA Match? Daily Updates Here September 2020 5
The Origins of Zana of Abkhazia July 2021 6
Full or Half Siblings April 2019 7 15
Ancestry Rearranged the Furniture January 2022 8
DNA from 459 Ancient British Isles Burials Reveals Relationships – Does Yours Match? February 2022 9
DNA Inherited from Grandparents and Great-Grandparents January 2020 10
Ancestry Only Shows Shared Matches of 20 cM and Greater – What That Means & Why It Matters May 2022 11
How Much Indian Do I Have in Me??? June 2015 12 8
Top Ten RootsTech 2022 DNA Sessions + All DNA Session Links March 2022 13
FamilyTreeDNA DISCOVER Launches – Including Y DNA Haplogroup Ages June 2022 14
Ancient Ireland’s Y and Mitochondrial DNA – Do You Match??? November 2020 15

2023 Suggestions

I have a few articles already in the works for 2023, including some surprises. I’ll unveil one very soon.

We will be starting out with:

  • Information about RootsTech where I’ll be giving at least 7 presentations, in person, and probably doing a book signing too. Yes, I know, 7 sessions – what was I thinking? I’ve just missed everyone so very much.
  • An article about how accurately Ancestry’s ThruLines predicts Potential Ancestors and a few ways to prove, or disprove, accuracy.
  • The continuation of the “In Search Of” series.

As always, I’m open for 2023 suggestions.

In the comments, let me know what topics you’d like to see.

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You Can Help Keep This Blog Free

I receive a small contribution when you click on some of the links to vendors in my articles. This does NOT increase the price you pay but helps me to keep the lights on and this informational blog free for everyone. Please click on the links in the articles or to the vendors below if you are purchasing products or DNA testing.

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The Ancestors are SPEAKing: An 18-Year Y-DNA Study That Led Us Home – 52 Ancestors #381

In 2004, 18 years ago, I founded the Speak(e)(s) Family DNA Project at FamilyTreeDNA. I descend from Nicholas Speaks through his son, Charles Speaks.

Some two decades before, I had met my wonderful cousin, Dolores Ham, by snail mail. We were introduced by Mary Parkey (1927-2000), a genealogist in the Cumberland Gap region who seemed to know something, if not everything, about the early settler families.

Mary wasn’t my cousin through the Speaks line, but she knew who was researching each line, and put me in touch with Dolores.

I met other researchers and discovered that a Speaks Family Association (SFA) had been formed in 1979.

I had a young family at the time, so I joined, but never attended any of the annual meetings, known as conventions, until 2005. I did enjoy the newsletters, however. It was always a good day when a newsletter or a letter from a cousin was waiting in the mailbox.

The goal of the Association was to share research and to determine if, and how, the various Speak lines in America were related. The “rumor” was that the family was from England, but no one knew for sure. We didn’t even know who was actually “in” the family, or how many different families there might be.

In 2004, when I established the Speaks DNA Project in collaboration with the SFA, our goal was stated, in part, as follows:

This project was begun to determine the various Speak(e)(s) lines around the world. According to family legend, the original ancestor came to England with William the Conqueror and his last name then was L’Espec. It was later spelled Speke and then the derivatives of Speake, Speakes, and Speaks carried by descendants today.

We knew that there was a Speak family in St. Mary’s County, Maryland.

Did our ”Nicholas” line descend from Maryland, or not?

We knew there was a Thomas Speak (c1634-1681) who settled there by 1661 and had two sons, John the InnKeeper or InnHolder (1665-1731) and Bowling (c1674-1755), named after his mother’s birth surname.

Fast forwarding two or three generations, our Nicholas Speak or Speaks was born about 1782 and was first found in Washington County, Virginia in 1804 when he married Sarah Faires. That’s a long way from Maryland. Who was Nicholas? Who were his parents? How did Nicholas get to Washington County, Virginia? There aren’t any other Speaks men, or women, in Washington County. Was he dropped fully grown by the stork?

In 2005, I attended my first Speaks Family Association Convention, held in Grand Rapids, Michigan, and met my lovely cousins who I’m quite close to. I gave an introductory talk about Y-DNA, and several Speaks males volunteered to test, including a descendant of Nicholas.

I was ecstatic, but within a year, we had a, well, “problem.”

In 2006, the Convention was held in Alabama, in the heat of summer. Not only did we have technology issues and lose power during the presentation, part of me hoped it wouldn’t come back on.

At that point, we had 8 Y-DNA testers.

At first, everything was fine. Two testers each from Thomas the immigrant through sons John and Bowling.

  • Thomas, Bowling and then two different sons. They matched.
  • Thomas, John, and his son Richard. They matched too.
  • All four men above, match each other.

Everything’s good, right?

Not so fast…

Then, a father/son pair tested who were also supposed to descend from the Thomas, Bowling, and Thomas line. Thankfully, they matched each other, but they did NOT match the other descendants of Thomas the immigrant.

Because we had multiple men through both of Thomas the immigrant’s sons, we had confirmed the Y-DNA STR marker signature of Thomas – which means that the father/son pair had experienced a genetic disconnect, or, they were actually descended from a different Speak line.

That wasn’t all though. Two more men tested who believed they descended from Thomas the immigrant through John and then Richard. They didn’t match each other, nor any of the other men either.

This was a difficult, painful situation, and not what was anticipated. Of course, I reviewed the results privately with the men involved before presenting them at the convention, and only did so with their permission.

In an effort to identify their genealogical lines, we discovered seven other mentions of early colonial Speak immigrants, including one named Thomas.

Over time, we would discover additional Y-DNA genetic Speak lines.

Bonus Cousin

Y-DNA also revealed an amazing new cousin, Henry, who didn’t know who his father was, but thanks to DNA, discovered he is a genetic Speaks AND identified his father.

Unfortunately, his father had recently passed away, but Henry contacted his uncle and was welcomed into his immediate family, as well as our broader Speaks family. Talk about life-changing! I will never, ever forget Henry’s emotional journey, or the small role I was privileged to play. For a long time, I couldn’t even tell his story without tearing up.

I met Henry in person for the first time at the convention last week. Lots of hugs all around!

In 2006, our Y-DNA haplogroup was known only as I1b1. We knew it was fairly rare and found in the rough Dinaric Alps border region between Bosnia and Croatia.

By User:Doron – Own work, CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=1551217

We weren’t wrong. We were just early. Our ancestors didn’t stop in the Alps.

Today, the migration path into Europe-proper looks like this.

In 2009, the convention was held in the Speaks Chapel United Methodist Church founded by the Reverend Nicholas Speaks, in Lee County, Virginia.

My dear cousin, Lola Margaret Speak Hall descends from Nicholas through two of his children and visited us as Nicholas’s wife, Sarah Faires, describing their lives together.

I can’t even begin to describe how moving it was to hear “Sarah” read from her Bible and recall her life with Nicholas and each of their children, especially those she buried across the road in the cemetery.

The cemetery was visible through the door as Sarah was speaking, describing Nicholas preaching their children’s funerals, and the sound of the clods of dirt hitting their coffins.

That reunion in Nicholas’s church was memorable for another reason, too. I was baptized, surrounded by my family, in my ancestor’s church.

Progress

More Speaks men were taking Y-DNA tests, but we still had no idea where the Speaks line originated overseas.

The Association had been working with John Speake in Cambridge, England, above, who had been assisting the American Speak family by obtaining British records. We had hoped that we would match his Y-DNA, because that would mean that we shared a common ancestor, probably from Priestweston, Shropshire in the 1500s. Plus, we really liked John and wanted to be related.

Sadly, that wasn’t the case, so we knew one English family we did NOT descend from, but we still didn’t know where our family line was from. We are, however, eternally grateful to John for his amazing research and the critical role he would play.

The Holy Grail

The Holy Grail of Y-DNA testing is often a match with a man either from the “old country,” wherever that is, or someone who unquestionably knows where their ancestor is from. Through a match with them, it allows other testers to jump the pond too.

In early 2010, John Speake in Cambridge reached out to me and said that he had found an anonymous man in New Zealand who was agreeable to taking a DNA test.

By this time, I wasn’t terribly hopeful, but John sweetened those waters by telling me that this man’s family had only been in New Zealand for two generations – and he knew where his ancestors “back home” were from.

I ordered a test for our anonymous tester.

I had nearly forgotten about this man a few weeks later when I suddenly received what seemed like a slot machine jackpot clanging when an entire series of emails arrived, one for each of our Y-DNA testers, saying they had a new match. Yep, our anonymous NZ tester.

Suddenly, I cared a whole lot about his genealogy.

Where was his paternal ancestral line from?

Gisburn.

Gisburn? Where the heck was Gisburn?

Gisburn

Gisburn is a tiny village in Lancashire, England.

This antiquarian map shows “Gisborn” located along the Ribble River. Gisburn is ancient, located on the old Roman road, appears in the Domesday Book of 1086 as Ghiseburne, and is believed to have been established in the 9th century.

This was beginning to get serious. This is no longer speculation or unsourced oral history, but actual evidence.

Another cousin, Susan Speake Sills, a DAR Chapter Regent, started digging immediately. Nothing motivates genealogists like the imminent hope of breaking down a brick wall.

Susan and I shot emails back and forth, night and day, for three or four days, and confirmed that our New Zealand cousin’s ancestor, James Speak, had been born in Gisburn between 1735-1749.

We knew, or though we knew, that Thomas Speake, the immigrant, was Catholic. Maryland was a safe haven for Catholics hoping to escape persecution in England.

Thomas was rumored to have been born to a John, but we had no idea where that rumor arose.

Was our Thomas born in Gisburn too?

Susan discovered that St. Mary’s Church in Gisburn held 50 marked Speaks burials.

In 1602/03, William in Gisburn had a son named John.

We found men named Richard, Stephen, John, William, Thomas and more.

And, there were many unmarked graves and unreadable stones.

Susan was just getting started.

Next, Susan discovered that the records of St. Mary’s and All Saints Church in Whalley held pages and pages of Speak family records.

The earliest Speak burial there was in 1540.

During this timeframe, people did not have the right to come and go freely. They were vassals, tied to the land.

Whalley is 11 miles from Gisburn.

Susan and I were fairly quiet as we worked, because we did NOT want to start any unfounded rumors by speaking too soon in the heat of our excitement. We were desperately trying to connect elusive dots.

In 2011, the Convention was held near Thomas and Bowlng Speak’s land in St. Mary’s County, Maryland, our ancestral homeland in America.

Thomas the immigrant settled in Port Tobacco sometime before 1661 and would have attended St. Ignatius Church at St. Thomas Manor where he was probably buried after his death in 1681, in what is now an unmarked grave.

I wonder if Thomas stood in the churchyard, perhaps during funerals, and gazed out over the Port Tobacco River which of course empties into the Chesapeake Bay, and wondered about the family members he had left behind, across the expansive ocean.

Thomas willed his land to his eldest son, John, who was an InnKeeper in Port Tobacco.

His younger son, Bowling Speak had to secure land on his own. He obtained land generally known as Zachia Manor.

This portion of the grant was specifically called “The Mistake,” although we have no idea why, which is owned in part today by St. Peter’s Catholic Church.

The land where the church actually stands was not owned by Bowling, just the attached land beginning about where the bus is parked and extending into the woods beside Jordan’s Run.

The old St. Peter’s cemetery, where the original church stood, is located nearby, just outside the boundary of Bowling and his son, Thomas of Zachia’s land.

It’s likely that our ancestors, Bowling and his son, Thomas, who died in 1755, within days of each other, and their wives, are buried here.

We gathered on Bowling’s land called Speaks Enlargement, adjacent The Mistake. It felt like Nirvana to have located his land and obtained permission to visit both parcels.

Me, Susan Speake Sills, Lola-Margaret Speak Hall and Joyce Candland, a descendant of John the InnKeeper, standing on Bowling’s land. We laughed so much that day as we explored Bowling and Thomas’s land, cherishing our time together.

Lola-Margaret’s heart-felt kiss of gratitude for this discovery says it all – for all of us. The only difference is that she actually had the hutzpah to do this!

Cousins on the prowl. What would we discover?

Susan found old, unmarked graves in the woods.

Lola-Margaret and I found rocks that had once been owned by Thomas and Bowling.

In 2011, my Convention presentation contained a surprise – the information about our Gisburn match, and what we had found. Church records, and graves.

I showed this cemetery map from St. Mary’s in Gisburn, where our New Zealand cousin’s family was buried.

It felt like we were so excruciatingly close, but still so far away.

We knew unquestionably that we were in the neighborhood, but where was our Thomas born?

Who was his family?

I closed with this photo of St. Mary’s in Gisburn and famously said, “I don’t know about you, but I want to stand there.”

It was a throw-away comment, or so I thought, but as it turned out, it wasn’t.

2013 – The Trip Home

Gisburn

Cousins Susan and Mary Speaks Hentschel left no stone unturned. Two years later, our Convention was held in Lancashire, and indeed, I got to stand there.

So did our Speak cousin from New Zealand whose Y-DNA test bulldozed this brick wall for us.

We were then, and remain, incredibly grateful for this amazing opportunity.

Of course, I couldn’t resist the St. Mary’s cemetery, nor the cemeteries at the other churches we would visit. It must be something about being a genealogist. There are still Speak family members being buried here.

There are many ancient and unmarked graves as well.

With abundant rainfall, cemeteries overgrow quickly.

It’s common for stones to be moved to the side, or even built into a wall, in order to facilitate maintenance of the grounds.

St. Mary’s church itself was built as a defensive structure sometime before 1135 with these arrowslits for archers in many locations, including the tower.

The Stirk House

During our visit, we stayed at the beautiful Stirk House in the Ribble Valley, a 17th century manor house and the only local lodging available for a group.

We discovered after we checked in that the Speak family had owned this property in the 1930s and had converted it into a hotel. How lucky could we be? Talk about synchronicity!

The Stirk House was originally built in 1635 using stone from the dismantled Sawley Abbey during Henry VIII’s reign and the resulting dissolution of the monasteries. Our Catholic ancestors would have witnessed this devastation, and probably grieved the destruction deeply.

For some reason, I was incredibly moved as we passed the remains of Sawley Abbey during our visit, and grabbed a shot through the rain-speckled window. At this point, I had no inkling of the historical connection that would emerge.

Whalley Abbey

Whalley Abbey, above, was destroyed as well in the Protestant attempt to eradicate Catholicism. Instead, they succeeded in driving it underground.

As our ancestors’ lives revolved around churches and religion, so did our visit as we retraced their steps through time.

While the stones of Sawley Abbey were repurposed to build local structures after its destruction, the Whalley Abbey and cloister walls, above, still stand, albeit in ruins.

The Abbey, formed in 1178, is shown in ruins here in this 1787 drawing. The village of Whalley is visible in the background, at right, with the church tower evident.

The Abbey spring, believed by some to be sacred, is fenced for protection today.

This trip was truly the opportunity of a lifetime and we tried to take advantage of every minute, absorbing everything our ancestors would have experienced, walking in their footsteps.

I didn’t fully grasp at that time that we weren’t hunting for “the” location or locations where our ancestors trod, but that they trod everyplace here. Wherever we walked, it was in their footsteps.

St. Mary’s Church in Whalley

Our next stop was St. Mary’s Church in Whalley, not far from the Abbey, where Henry Speke was granted a lease in 1540.

This church is ancient, build in the 1200s, replacing an earlier church, and stunningly beautiful.

Our trip group photo was taken inside St. Mary’s.

As we sat in the choir, our guide explained the history of the church, which is our history too.

The little green men carved into the wooden choir seats are a wink and a nod to an earlier pagan era. Our ancestors would have known that era too.

We sat in the pews where earlier generations of Speaks families sat. The boxed, enclosed pews were for the wealthy manor owners. Our family wouldn’t have been sitting there.

The original St. Mary’s church, shown in this painting, looked different than today. The church in the painting would have felt quite familiar to the early Speak families who sat in the pews here each Sunday.

In addition to the churches in Gisburn and Whalley, we visited St. Leonard’s Church in Downham which is a chapelry of the church in Whalley.

Downham

The tower is original to the 1400s, but the rest of the church was rebuilt in 1909-10. Lord Clitheroe graciously brought a drawing of the old church as it looked when the Speak family attended.

This church, in the shadow of Pendle Hill, proved to be quite important to the family.

Pendle Hill from the cemetery outside St. Leonard’s church, where Thomas was baptized.

Pendle Hill can be seen across the roofs of the village houses.

Downham, on the north side of Pendle Hill was small then, and remains a crossroad village today with a population of about 150 people, including Twiston.

Twiston is located less than 3 miles away, yet it’s extremely remote, at the foot or perhaps on the side of Pendle Hill.

What’s left of the stocks at Downham, beside the church cemetery, just waiting for those who needed to be punished, like those reviled Catholics hiding out in the wilds over by Pendle Hill.

During our visit, Lord Clitheroe provided us with a transcription of the Downham church records wherein one Thomas Speak was baptized on January 1, 1633/34, born to Joannis, the Latin form of John, in nearby Twiston.

Is this Thomas our Thomas the immigrant who was born about that same time? We still don’t know, but there are clues.

The problem is that there is a marriage record for a Thomas Speak to Grace Shakelford in 1656, and a burial record in 1666 for Grace recorded as “the wife of Thomas Speak of Twiston.” But there is no burial record for Thomas, and no children recorded either during that time, which is very strange.

So, is that our Thomas, or a different Thomas? Those records don’t align well. It’s certainly a Thomas of the right age, in the right place, and born to a John as well.

However, our Thomas was in Maryland by at least 1661 and probably earlier. Would he have left a wife behind? Would she still have been noted as his wife and him recorded as “of Twiston” if he was in America?

Records in this area are incomplete. A substantial battle was fought in Whalley in 1643. Churches were often used for quartering soldiers. Minister’s notes could well have been displaced, or books destroyed entirely.

In Downham, the years of 1608-1619 are missing, along with 1638-1657, inclusive which would hold records vital to our family for nearly two critical decades.

We know, according to probate records, that the Downham families originated in Whalley based on research by John D. Speake, of Cambridge, contained in the recently published book, The Speak/e/s Family of Southern Maryland

Probate files show that in 1615, “John Speake of Twiston, husbandman” mentions his son William and William’s children, including John who was the administrator of his will. For John to be an administrator, he had to be age 21 or over, so born in 1594 or earlier. Some John Speak married Elizabeth Biesley at Whalley in 1622 and is believed to be the John Speak Sr. recorded in Downham Parish Registers.

However, John seemed to be the Speak given name of choice.

The existing Hearth Tax returns for 1666-1671 that recorded, and taxed, the number of hearths observed in each home during an inspection shows the following Speak households, none of which were too impoverished to have a hearth:

  • 3 in Twiston
  • 2 in Gisburn (Remington)
  • 1 in Stansfield, near Halifax

Of the above entries, 5 were named John, and one was Ann.

There were two additional Speak families in Newchurch, near Pendle, which is more distant, as is Stansfield, maybe a total of 30 miles end-to-end.

There were no Thomas Speaks listed.

One final hint may be that there are three tailors mentioned in the Gisburn church registers over time, one of whom was Thomas, a tailor, who died in 1662. Did our Thomas the immigrant come from a long line of tailors? If so, how could he have supported himself as a tailor in the remote Lancashire countryside? Is that, perhaps, part of why he immigrated, in addition to being Catholic?

Or, maybe our Thomas apprenticed as a tailor in Maryland as an indentured servant and tailors in Gisburn are simply a red herring.

The Whalley, Gisburn and Twiston families are closely connected. The difference may well be that our Thomas’s line remained secretly Catholic, so preferred the “uninhabited” areas of the remote Twiston countryside. Even today, Gisburn is described as being “rural, surrounded by hilly and relatively unpopulated areas.” And that’s Gisburn, with more than 500 residents. Downham is much smaller, about 20% of the size of Gisburn.

What do we know about Twiston?

Twiston

Twiston is too small to even be called a hamlet. These ghostly buildings are what’s left of the former Twiston Mill, built after an earlier mill burned in 1882. The original farm and corn mill was owned originally by Whalley Abbey at least since the 1300s. Twiston is near an old lime kiln, probably in use since Roman times, and the Witches Quarry, a steep, vertical rocky outcrop popular with hikers and rock climbers.

The ancient homesteads were clustered along the bubbling Twiston Brook, a branch of Pendle Brook that originates on Pendle Hill, watering the farm and powering the original corn mill. It was actually a smart place to settle, because the stream was fresh, given that there were no upstream homesteads to pollute the water.

These buildings stood, huddled together, probably for safety, in a field carved out of the wilderness, surrounded today by hundreds of sheep grazing on the hillsides and high moors.

Stone walls divide pastures and line the steep hillsides, with gates allowing shepherds and now, farmers to pass through. Eventually, the sheep venture high enough to graze and shelter on the moorland.

At the higher levels of Pendle Hill, the forest gives way to moors and the sheep roam freely.

The sheep also have the right-of-way, so vehicles travel slowly. The heathered moor is quite stark and incredibly beautiful.

The fields along the Ribble River with its feeder brooks and settlements, running through the valley beneath Pendle Hill are lush, green, and timeless. The land surrounding the River is relatively flat, beckoning settlers and encouraging farming.

This is one of those places where the ancient voices call out and pluck the strings of your heart.

And your heart answers in recognition.

Where you know the earth holds the DNA of your ancestors, and their blood watered the landscape in the Ribble Valley.

By Beacon Hill overlooking the Ribble valley by Bill Boaden, CC BY-SA 2.0, https://commons.wikimedia.org/w/index.php?curid=106624444

Beacon Hill overlooks the Ribble Valley, with Pendle Hill in the background.

Our ancestors lived, and loved here and because of that, we live now.

Their descendants are scattered across the world, on many continents, yet we reunited here in our homeland – like birds following their sacred compass, guiding them across the oceans home again.

When the Speak family lived here, it was considered a “wild and lawless region” by local authorities, probably due in part to its remoteness – and also the rebellious nature of the inhabitants. We have never submitted easily to pressure.

Twiston is nestled at the base of Pendle Hill.

If you were a Catholic, living in a hotbed of “recussants,” and trying to be invisible, Twiston would be a location where you might be able to successfully disappear among those of like mind.

The road to Twiston was too twisty, rock-lined and narrow for our bus to navigate, causing us to have to back up down a one lane road with rock walls on both sides for some distance.

These ancient moss and fern-covered walls have stood for centuries, some with gateway passages to neighboring houses in small hamlets.

Others stand sentry along the old cartways where they’ve been for centuries.

The stone walls keep sheep and cattle in, and today, wayward vehicles out.

The walls have been tended and repaired by generations of stewards. Generations of our Speaks men probably placed some of these very stones, having removed them from their fields.

The footpaths, now roads, pass within inches of old stone homes and barns, dissecting farms in many places. That’s exactly how the old cart road traveled, and how you got to your neighbor’s farm. In fact, that old road took you right to their door.

Pendle Hill always serves as your guidepost.

If you’re lost and don’t know which way to turn, just find the hill and reorient yourself.

Its stark beauty is ever-present. Pendle Hill always looms someplace in the distance.

Since the bus couldn’t get to Twiston, a few adventurous cousins somehow found a taxi to rent and a brave driver willing to take them to Twiston, after he finally figured out where Twiston actually was.

I’m still REALLY mad at myself because I took a hike in the forest instead, although I enjoyed connecting with the land.

It had been a very long day and I didn’t really realize the significance of Twiston at that time. Plus, space in the taxi was limited and I suffer from motion sickness. I should have taken Dramamine, sat on the roof, and gone anyway.

The road to Twiston, now called a lane, grows increasingly narrow. Who knew there was such a remote region in the hill country of Lancashire?

Finally, Twiston appears where the forest ends and the road widens a tiny bit.

If only these ancient buildings and rock walls could speak, share their stories and reveal their secrets. Old documents, however, do provide some insight.

This document, originally penned in Latin, was provided by the Lancashire archives.

John Speak, in 1609, was a farmer, with a house (messauge), garden, orchard, 10 acres of farmland, 5 of meadow, and 10 acres of pasture.

Even orchards were walled to prevent unwanted visitors.

Indeed, Twiston is where John Speak lived. If the Thomas born in Twiston to Joannis, Latin for John, in 1633 and baptized on January 1, 1634 in old St. Leonard’s Church in Downham is our Thomas, this is his birth location.

For our family, this is, indeed, hallowed ground.

Catholics weren’t the only people sheltering in the shadow of Pendle Hill.

The accused Pendle Witches, probably women who were traditional healers, lived here too, persecuted and executed in 1612, as did Quakers, all vilified along with Catholics.

No wonder Thomas, along with the Catholic Bowling family, found a way to make his way to the safety of Maryland.

It’s ironic that in 1670, after being persecuted themselves for their Catholic beliefs, in this same valley, the Speake men were reporting Quakers.

Records of Speak men in Twiston persist into the 1800s, and one of our local testers descends from Henry Speake, born about 1650 in Twiston.

Local Testers

Prior to our visit, we published small ads in local newspapers and contacted historical societies. We found several Speak(e)(s) families and invited them to dinner at the Stirk House where the after-dinner speaker explained all about DNA testing. You probably can’t see them clearly, but there are numerous DNA kits laying on the table, just waiting for people to have a swab party.

Our guests brought their family information and photos and we had an absolutely lovely evening.

One of those families traced their line to Twiston. Be still my heart.

Five men from separate Speak families tested. None of them knew of any connection between their families, and all presumed they were not related.

I carried those men’s DNA tests back in my hand luggage like the gold that they were.

They were wrong. All five men matched each other, AND our Thomas Speake line. Susan and I got busy connecting the dots genealogically, as much as possible

  • Two of our men descended from Henry born in 1650, married Alice Hill and lived in Downham/Twiston.
  • Two of our men descended from John Speak born about 1540, married Elina Singleton, and lived in Whalley.
  • Two of our men, including our New Zealand tester, descend from John born sometime around 1700, probably in Gisburn where his son, James, was born about 1745.

We knew indeed that we had found our way “home.”

2022

Today, the Speaks family DNA Project has 146 members comprised of:

  • 105 autosomal testers
  • 31 Speak Y-DNA testers
  • 24 of whom are Thomas the immigrant descendants
  • 8 Big Y tests

Over the years, we’ve added another goal. We need to determine how a man named Aaron Lucky Speaks is related to the rest of us. Autosomal DNA confirms that he is related, but we need more information.

Aaron Lucky is first found in 1787 purchasing land and on the 1790 Iredell County, NC census. We finally located a Y-DNA tester and confirmed that his paternal line is indeed the Lancashire Speaks line, but how?

After discovering that all 5 Lancashire Speaks men descend from the same family as Thomas the immigrant, we have spent a great deal of time trying to both sort them out, and tie the family lines together, with very limited success.

Can Y-DNA do that for us?

The Y-DNA Block Tree

When men take a Big Y-700 DNA test, they receive the most detailed information possible, including all available STR markers plus the most refined haplogroup possible, placing them as a leaf on the very tip of their branch of the tree of mankind. The only other men there are their closest relatives, divided sometimes by a single mutation. Eight Speaks men have taken or upgraded to the Big Y test, providing information via matching that we desperately needed.

This Big Y block tree is from the perspective of a descendant of Nicholas Speaks and shows the various mutations that define branches, shown as building blocks. Each person shown on the Block Tree is a match to the tester.

Think of haplogroups as umbrellas. Each umbrella shelters and includes everything beneath it.

At the top of this block tree, we have one solid blue block that forms an umbrella over all three branches beneath it. The top mutation name is I-BY14004, which is the haplogroup name associated with that block.

We have determined that all of the Speak men descended from the Lancashire line are members of haplogroup I-BY14004 and therefore, fall under that umbrella. The other haplogroup names in the same block mean that as other men test, a new branch may split off beneath the branch.

Next, let’s look at the blue block at far left.

The Lancashire men, meaning those who live there, plus our New Zealand tester, also carry additional mutations that define haplogroup I-BY14009, which means that our Thomas the Immigrant line split off from theirs before that mutation was formed.

Thomas the immigrant’s line has the mutation defining haplogroup I-FTA21638, forming an umbrella over both of Thomas the immigrant’s sons – meaning descendants of both sons carry this mutation.

Bowling’s line is defined by haplogroup I-BY215064, but John’s line does not carry this mutation, so John’s descendants are NOT members of this haplogroup, which turns out to be quite important.

We are very fortunate that one of Thomas’s sons, Bowling, received a mutation, because it allows us to differentiate between Bowling and his brother, John’s, descendants easily if testers take the Big Y test.

Aaron Luckey Speak

As you can see, the descendants of Aaron Lucky Speak, bracketed in blue above, carry the Bowling line mutation, so Aaron Luckey descends from one of Bowling’s sons. That makes sense, especially since Charles, the father of Nicholas, my ancestor born in 1782, is also found in Iredell County during the same timeframe.

Here’s a different view of the Big Y testers along with STR Y-DNA testers in a spreadsheet that I maintain.

Thomas the immigrant (tan band top row) is shown with son, Bowling who carries haplogroup BY215064.

Thomas’s son John, the InnKeeper, shown in the blue bar does NOT have the BY215064 mutation that defines Bowling’s group.

However, the bright green Aaron Lucky line, disconnected at far right, does have the mutation BY215064, so this places Aaron Luckey someplace beneath, meaning a descendant of, Bowling. We just don’t know where yet.

Sometimes we can utilize STR marker mutations for subgrouping within haplogroups, but in this case, we cannot because STR mutations in this family have:

  • Occurred independently in different lines
  • Back mutated

Between both of these issues, STR mutations are inconsistent and entirely unreliable.

In some cases, autosomal DNA is useful, but in this case, autosomal doesn’t get us any closer than Y-DNA due to record loss and incomplete genealogy above Nicholas. An analysis shows that Aaron Luckey Speak’s descendants match each other closer than they match either John or Bowling’s descendants.

We have a large gap in known descendants beneath Thomas of Zachia, other than Nicholas’s line.

Combining genetic and genealogy information, we know that both Charles Beckworth Speak and Thomas Bowling Speak, in yellow, are found in Iredell County. The children of Thomas of Zachia, shown in purple, are born in the 1730s and any one of them could potentially be the father of Aaron Luckey.

The men in green, including William, Bowling’s other son, are also candidates to be Aaron Luckey’s ancestor, although the two yellow men are more likely due to geographic proximity. They are both found in Iredell County.

We don’t know anything about William’s children, if any, nor much about Edward. John settled in Kentucky. Nicholas (green) stayed in Maryland.

There may be an additional generation between Charles Beckworth Speak (yellow) and Nicholas (born 1782), also named Charles. There’s a lot of uncertainty in this part of the tree.

Aaron Luckey’s descendants may be able to search their matches for a Luckey family, found in both Iredell County AND Maryland, which may assist with further identification.

It seems that Aaron’s middle name of Lucky is likely to be very significant.

Connecting the Genetic Dots in England

What can we discern about the Speak family in the US and in Lancashire?

Reaching back in time, before Thomas was born about 1633, what can we tell about the Speak family and how they are connected, and when?

The recently introduced Discover tool allows us to view the Y-DNA haplogroups and when they were born, meaning when the haplogroup-defining mutation occurred.

The Time Tree shows the haplogroups, in black above the profile dots. The scientifically calculated approximate dates of when those haplogroups were “born,” meaning when those mutations occurred, are found across the top.

I’ve added genealogical information, in red, at right.

  • Reading from the bottom red dot, Bowling’s haplogroup was born about the year 1660. Bowling was indeed born in 1674, so that’s VERY close
  • Moving back in time, Thomas’s haplogroup was born about 1617 and Thomas himself was born about 1634, but it certainly could have been earlier.
  • The Lancashire testers’ common haplogroup was born about 1636, and the earliest known ancestor of those men is Henry, born in Twiston in 1650.
  • The common Speak ancestor of BOTH the Lancashire line and the Thomas the immigrant line was born about 1334. The earliest record of any Speak was Henry Speke, of Whalley, born before 1520.

The lines of Thomas the Immigrant and the Lancashire men diverged sometime between about 1334, when the umbrella mutation for all Speaks lines was born, and about 1617 when we know the mutation defining the Thomas the Immigrant line formed and split off from the Lancashire line.

But that’s not all.

Surprise!

As I panned out and viewed the block tree more broadly, I noticed something.

This is quite small and difficult to read, so let me explain. At far left is the branch for our Speaks men. The common ancestor of that group was born about 1334 CE, meaning current era, as we’ve discussed.

Continuing up the tree, we see the next haplogroup umbrella occurs about 1009 CE, then the year 850 at the top is the next umbrella, encompassing everything beneath.

Looking to the right, the farthest right blocks date to 1109 CE, then 1318 CE, then progressing on down the tree branch to the bottom, I see one name in three blocks.

What is that name?

I’m squinting!!!

Here, let me enlarge this for you!

Standish.

The name is Standish, as in Myles Standish, the Pilgrim.

Miles is our relative, and even though he has a different surname, we share a common ancestor, probably before surnames were adopted. Our genetic branches divided about the year 1000.

The Discover tool also provides Notable Connections for each haplogroup, so I entered one of the Speaks haplogroups, and sure enough, the closest Speak Notable Connection is Myles Standish 1584-1656.

And look, there’s the Standish Pew in Chorley, another church that we visited during our Lancashire trip because family members of Thomas Speake’s wife, Elizabeth Bowling, are found in the church records here.

Our common ancestor with the Standish line lived in about the year 850. Our line split off, as did theirs about the year 1000, or about 1000 years, or 30-40 generations ago.

Our family names are still found in the Chorley Church records

Ancient Connections

The Discover tool also provides Ancient Connections from archaeological digs, by haplogroup.

Sure enough, there’s an ancient sample on the Time Tree named Heslerton 20641.

Checking the Discover Ancient Connections, the man named Heslerton 20641 is found in West Heslerton, Yorkshire and lived about the year 450-650, based on carbon dating.

The mutation identifying the common ancestor between the Speak men and Heslerton occurred about 2450 BCE, or 4500 years ago. Those two locations are only 83 miles apart.

Where Are We?

What have we learned from the information discovered through genealogy combined with Big Y testing?

  • We found a Speek in Whalley in 1385.
  • Thomas Speake was baptized in Downham and born in Twiston in 1733.
  • Our New Zealand tester’s ancestor was found in Gisburn about 1745.
  • All of these locations are within 15 miles of each other.

  • Chorley, where the Standish family is found in the 1500s is located 17 miles South of Whalley. Thomas Speak’s wife, Elizabeth Bowlings’ family is found in the Chorley church records.

What about the L’Espec origin myth?

  • The Speak family clearly did not arrive in 1066 with the Normans.
  • We have no Scandinavian DNA matches.
  • No place is the surname spelled L’Espec in any Lancashire regional records.
  • The Speak family is in Whalley/Chorley area by 1000 when the Speak/Standish lines diverged
  • The common ancestor with the Standish family occurred about the year 850, although that could have occurred elsewhere. Clearly, their common ancestor was in the Chorley/Whalley area by 1000 when their lines diverged.

The cemetery at Whalley includes Anglo-Saxon burials, circa 800-900.

The Speak men, with no surname back then, greeted William the Conqueror.

And lived to tell the tale, along with their Standish cousins, of course.

Are our ancestors buried in these early Anglo-Saxon graves? I’d wager that the answer is yes. We are likely related to every family who lived in this region over many millennia. Little is known of Lancashire during this time, but we do know more generally that the Anglo-Saxons, a Germanic people, arrived in the 5th century and integrated, eventually, with the Native Britons, the Celts. These carvings certainly do have a Celtic feel.

This family photo, standing in the church in Whalley where it all began, is now imbued with a much deeper significance.

Little did we know.

And this, all of this, was a result of Big-Y DNA tests. We could not have accomplished any of this without Y-DNA testing.

Our ancestors are indeed speaking across the ages.

We really have found the road home, the path revealed by the DNA of our ancestors.

_____________________________________________________________

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DNA: In Search of…Signs of Endogamy

This is the fourth in our series of articles about searching for unknown close family members, specifically; parents, grandparents, or siblings. However, these same techniques can be applied by genealogists to ancestors further back in time as well.

In this article, we discuss endogamy – how to determine if you have it, from what population, and how to follow the road signs.

After introductions, we will be covering the following topics:

  • Pedigree collapse and endogamy
  • Endogamous groups
  • The challenge(s) of endogamy
  • Endogamy and unknown close relatives (parents, grandparents)
  • Ethnicity and Populations
  • Matches
  • AutoClusters
  • Endogamous Relationships
  • Endogamous DNA Segments
  • “Are Your Parents Related?” Tool
  • Surnames
  • Projects
  • Locations
  • Y DNA, Mitochondrial DNA, and Endogamy
  • Endogamy Tools Summary Tables
    • Summary of Endogamy Tools by Vendor
    • Summary of Endogamous Populations Identified by Each Tool
    • Summary of Tools to Assist People Seeking Unknown Parents and Grandparents

What Is Endogamy and Why Does It Matter?

Endogamy occurs when a group or population of people intermarry among themselves for an extended period of time, without the introduction of many or any people from outside of that population.

The effect of this continual intermarriage is that the founders’ DNA simply gets passed around and around, eventually in small segments.

That happens because there is no “other” DNA to draw from within the population. Knowing or determining that you have endogamy helps make sense of DNA matching patterns, and those patterns can lead you to unknown relatives, both close and distant.

This Article

This article serves two purposes.

  • This article is educational and relevant for all researchers. We discuss endogamy using multiple tools and examples from known endogamous people and populations.
  • In order to be able to discern endogamy when we don’t know who our parents or grandparents are, we need to know what signs and signals to look for, and why, which is based on what endogamy looks like in people who know their heritage.

There’s no crystal ball – no definitive “one-way” arrow, but there are a series of indications that suggest endogamy.

Depending on the endogamous population you’re dealing with, those signs aren’t always the same.

If you’re sighing now, I understand – but that’s exactly WHY I wrote this article.

We’re covering a lot of ground, but these road markers are invaluable diagnostic tools.

I’ve previously written about endogamy in the articles:

Let’s start with definitions.

Pedigree Collapse and Endogamy

Pedigree collapse isn’t the same as endogamy. Pedigree collapse is when you have ancestors that repeat in your tree.

In this example, the parents of our DNA tester are first cousins, which means the tester shares great-grandparents on both sides and, of course, the same ancestors from there on back in their tree.

This also means they share more of those ancestors’ DNA than they would normally share.

John Smith and Mary Johnson are both in the tree twice, in the same position as great-grandparents. Normally, Tester Smith would carry approximately 12.5% of each of his great-grandparents’ DNA, assuming for illustration purposes that exactly 50% of each ancestor’s DNA is passed in each generation. In this case, due to pedigree collapse, 25% of Tester Smith’s DNA descends from John Smith, and another 25% descends from Mary Johnson, double what it would normally be. 25% is the amount of DNA contribution normally inherited from grandparents, not great-grandparents.

While we may find first cousin marriages a bit eyebrow-raising today, they were quite common in the past. Both laws and customs varied with the country, time, social norms, and religion.

Pedigree Collapse and Endogamy is NOT the Same

You might think that pedigree collapse and endogamy is one and the same, but there’s a difference. Pedigree collapse can lead to endogamy, but it takes more than one instance of pedigree collapse to morph into endogamy within a population. Population is the key word for endogamy.

The main difference is that pedigree collapse occurs with known ancestors in more recent generations for one person, while endogamy is longer-term and systemic in a group of people.

Picture a group of people, all descended from Tester Smith’s great-grandparents intermarrying. Now you have the beginnings of endogamy. A couple hundred or a few hundred years later, you have true endogamy.

In other words, endogamy is pedigree collapse on a larger scale – think of a village or a church.

My ancestors’ village of Schnait, in Germany, is shown above in 1685. One church and maybe 30 or 40 homes. According to church and other records, the same families had inhabited this village, and region, for generations. It’s a sure bet that both pedigree collapse and endogamy existed in this small community.

If pedigree collapse happens over and over again because there are no other people within the community to marry, then you have endogamy. In other words, with endogamy, you assuredly DO have historical pedigree collapse, generally back in time, often before you can identify those specific ancestors – because everyone descends from the same set of founders.

Endogamy Doesn’t Necessarily Indicate Recent Pedigree Collapse

With deep, historic endogamy, you don’t necessarily have recent pedigree collapse, and in fact, many people do not. Jewish people are a good example of this phenomenon. They shared ancestors for hundreds or thousands of years, depending on which group we are referring to, but in recent, known, generations, many Jewish people aren’t related. Still, their DNA often matches each other.

The good news is that there are telltale signs and signals of endogamy.

The bad news is that not all of these are obvious, meaning as an aid to people seeking clues about unknown close relatives, and other “signs” aren’t what they are believed to be.

Let’s step through each endogamy identifier, or “hint,” and then we will review how we can best utilize this information.

First, let’s take a look at groups that are considered to be endogamous.

Endogamous Groups

Jewish PeopleSpecifically groups that were isolated from other groups of Jewish (and other) people; Ashkenazi (Germany, Northern France, and diaspora), Sephardic (Spanish, Iberia, and diaspora), Mizrahi (Israel, Middle Eastern, and diaspora,) Ethiopian Jews, and possibly Jews from other locations such as Mountain Jews from Kazakhstan and the Caucasus.

AcadiansDescendants of about 60 French families who settled in “Acadia” beginning about 1604, primarily on the island of Nova Scotia, and intermarried among themselves and with the Mi’kmaq people. Expelled by the English in 1755, they were scattered in groups to various diasporic regions where they continued to intermarry and where their descendants are found today. Some Acadians became the Cajuns of Louisiana.

Anabaptist Protestant FaithsAmish, Mennonite, and Brethren (Dunkards) and their offshoots are Protestant religious sects founded in Europe in the 14th, 15th, and 16th centuries on the principle of baptizing only adults or people who are old enough to choose to follow the faith, or rebaptizing people who had been previously baptized as children. These Anabaptist faiths tend to marry within their own group or church and often expel those who marry outside of the faith. Many emigrated to the American colonies and elsewhere, seeking religious freedom. Occasionally those groups would locate in close proximity and intermarry, but not marry outside of other Anabaptist denominations.

Native American (Indigenous) People – all indigenous peoples found in North and South America before European colonization descended from a small number of original founders who probably arrived at multiple times.

Indigenous Pacific Islanders – Including indigenous peoples of Australia, New Zealand, and Hawaii prior to colonization. They are probably equally as endogamous as Native American people, but I don’t have specific examples to share.

Villages – European or other villages with little inflow or whose residents were restricted from leaving over hundreds of years.

Other groups may have significant multiple lines of pedigree collapse and therefore become endogamous over time. Some people from Newfoundland, French Canadians, and Mormons (Church of Jesus Christ of Latter-Day Saints) come to mind.

Endogamy is a process that occurs over time.

Endogamy and Unknown Relatives

If you know who your relatives are, you may already know you’re from an endogamous population, but if you’re searching for close relatives, it’s helpful to be able to determine if you have endogamous heritage, at least in recent generations.

If you know nothing about either parent, some of these tools won’t help you, at least not initially, but others will. However, as you add to your knowledge base, the other tools will become more useful.

If you know the identity of one parent, this process becomes at least somewhat easier.

In future articles, we will search specifically for parents and each of your four grandparents. In this article, I’ll review each of the diagnostic tools and techniques you can use to determine if you have endogamy, and perhaps pinpoint the source.

The Challenge

People with endogamous heritage are related in multiple, unknown ways, over many generations. They may also be related in known ways in recent generations.

If both of your parents share the SAME endogamous culture or group of relatives:

  • You may have significantly more autosomal DNA matches than people without endogamy, unless that group of people is under-sampled. Jewish people have significantly more matches, but Native people have fewer due to under-sampling.
  • You may experience a higher-than-normal cM (centiMorgan) total for estimated relationships, especially more distant relationships, 3C and beyond.
  • You will have many matches related to you on both your maternal and paternal sides.
  • Parts of your autosomal DNA will be the same on both your mother’s and father’s sides, meaning your DNA will be fully identical in some locations. (I’ll explain more in a minute.)

If either (or both) of your parents are from an endogamous population, you:

  • Will, in some cases, carry identifying Y and mitochondrial DNA that points to a specific endogamous group. This is true for Native people, can be true for Jewish people and Pacific Islanders, but is not true for Anabaptist people.

One Size Does NOT Fit All

Please note that there is no “one size fits all.”

Each or any of these tools may provide relevant hints, depending on:

  • Your heritage
  • How many other people have tested from the relevant population group
  • How many close or distant relatives have tested
  • If your parents share the same heritage
  • Your unique DNA inheritance pattern
  • If your parents, individually, were fully endogamous or only partly endogamous, and how far back generationally that endogamy occurred

For example, in my own genealogy, my maternal grandmother’s father was Acadian on his father’s side. While I’m not fully endogamous, I have significantly more matches through that line proportionally than on my other lines.

I have Brethren endogamy on my mother’s side via her paternal grandmother.

Endogamous ancestors are shown with red stars on my mother’s pedigree chart, above. However, please note that her maternal and paternal endogamous ancestors are not from the same endogamous population.

However, I STILL have fewer matches on my mother’s side in total than on my father’s side because my mother has recent Dutch and recent German immigrants which reduces her total number of matches. Neither of those lines have had as much time to produce descendants in the US, and Europe is under-sampled when compared with the US where more people tend to take DNA tests because they are searching for where they came from.

My father’s ancestors have been in the US since it was a British Colony, and I have many more cousins who have tested on his side than mother’s.

If you looked at my pedigree chart and thought to yourself, “that’s messy,” you’d be right.

The “endogamy means more matches” axiom does not hold true for me, comparatively, between my parents – in part because my mother’s German and Dutch lines are such recent immigrants.

The number of matches alone isn’t going to tell this story.

We are going to need to look at several pieces and parts for more information. Let’s start with ethnicity.

Ethnicity and Populations

Ethnicity can be a double-edged sword. It can tell you exactly nothing you couldn’t discern by looking in the mirror, or, conversely, it can be a wealth of information.

Ethnicity reveals the parts of the world where your ancestors originated. When searching for recent ancestors, you’re most interested in majority ethnicity, meaning the 50% of your DNA that you received from each of your parents.

Ethnicity results at each vendor are easy to find and relatively easy to understand.

This individual at FamilyTreeDNA is 100% Ashkenazi Jewish.

If they were 50% Jewish, we could then estimate, and that’s an important word, that either one of their parents was fully Jewish, and not the other, or that two of their grandparents were Jewish, although not necessarily on the same side.

On the other hand, my mother’s ethnicity, shown below, has nothing remarkable that would point to any majority endogamous population, yet she has two.

The only hint of endogamy from ethnicity would be her ~1% Americas, and that isn’t relevant for finding close relatives. However, minority ancestry is very relevant for identifying Native ancestors, which I wrote about, here.

You can correlate or track your ethnicity segments to specific ancestors, which I discussed in the article, Native American & Minority Ancestors Identified Using DNAPainter Plus Ethnicity Segments, here.

Since I wrote that article, FamilyTreeDNA has added the feature of ethnicity or population Chromosome Painting, based on where each of your populations fall on your chromosomes.

In this example on chromosome 1, I have European ancestry (blue,) except for the pink Native segment, which occurs on the following segment in the same location on my mother’s chromosome 1 as well.

Both 23andMe, and FamilyTreeDNA provide chromosome painting AND the associated segment information so you can identify the relevant ancestors.

Ancestry is in the process of rolling out an ethnicity painting feature, BUT, it has no segment or associated matching information. While it’s interesting eye candy, it’s not terribly useful beyond the ethnicity information that Ancestry already provides. However, Jonny Perl at DNAPainter has devised a way to estimate Ancestry’s start and stop locations, here. Way to go Jonny!

Now all you need to do is convince your Ancestry matches to upload their DNA file to one of the three databases, FamilyTreeDNA, MyHeritage, and GEDMatch, that accept transfers, aka uploads. This allows matching with segment data so that you can identify who matches you on that segment, track your ancestors, and paint your ancestral segments at DNAPainter.

I provided step-by-step instructions, here, for downloading your raw DNA file from each vendor in order to upload the file to another vendor.

Ethnicity Sides

Three of the four DNA testing vendors, 23andMe, FamilyTreeDNA, and recently, Ancestry, attempt to phase your ethnicity DNA, meaning to assign it to one parental “side” or the other – both in total and on each chromosome.

Here’s Ancestry’s SideView, where your DNA is estimated to belong to parent 1 and parent 2. I detailed how to determine which side is which, here, and while that article was written specifically pertaining to Ancestry’s SideView, the technique is relevant for all the vendors who attempt to divide your DNA into parents, a technique known as phasing.

I say “attempt” because phasing may or may not be accurate, meaning the top chromosome may not always be parent 1, and the bottom chromosome may not always be chromosome 2.

Here’s an example at 23andMe.

See the two yellow segments. They are both assigned as Native. I happen to know one is from the mother and one is from the father, yet they are both displayed on the “top” chromosome, which one would interpret to be the same parent.

I am absolutely positive this is not the case because this is a close family member, and I have the DNA of the parent who contributed the Native segment on chromosome 1, on the top chromosome. That parent does not have a Native segment on chromosome 2 to contribute. So that Native segment had to be contributed by the other parent, but it’s also shown on the top chromosome.

The DNA segments circled in purple belong together on the same “side” and were contributed to the tester by the same parent. The Native segment on chromosome 2 abuts a purple African segment, suggesting perhaps that the ancestor who contributed that segment was mixed between those ethnicities. In the US, that suggests enslavement.

The other African segments, circled, are shown on the second chromosome in each pair.

To be clear, parent 1 is not assigned by the vendors to either mother or father and will differ by person. Your parent 1, or the parent on the top chromosome may be your mother and another person’s parent 1 may be their father.

As shown in this example, parents can vary by chromosome, a phenomenon known as “strand swap.” Occasionally, the DNA can even be swapped within a chromosome assignment.

You can, however, get an idea of the division of your DNA at any specific location. As shown above, you can only have a maximum of two populations of DNA on any one chromosome location.

In our example above, this person’s majority ancestry is European (blue.) On each chromosome where we find a minority segment, the opposite chromosome in the same location is European, meaning blue.

Let’s look at another example.

At FamilyTreeDNA, the person whose ethnicity painting is shown below has a Native American (pink) ancestor on their father’s side. FamilyTreeDNA has correctly phased or identified their Native segments as all belonging to the second chromosome in each pair.

Looking at chromosome 18, for example, most of their father’s chromosome is Native American (pink). The other parent’s chromosome is European (dark blue) at those same locations.

If one of the parents was of one ethnicity, and the other parent is a completely different ethnicity, then one bar of each chromosome would be all pink, for example, and one would be entirely blue, representing the other ethnicity.

Phasing ethnicity or populations to maternal and paternal sides is not foolproof, and each chromosome is phased individually.

Ethnicity can, in some cases, give you a really good idea of what you’re dealing with in terms of heritage and endogamy.

If someone had an Ashkenazi Jewish father and European mother, for example, one copy of each chromosome would be yellow (Ashkenazi Jewish), and one would be blue (European.)

However, if each of their parents were half European Jewish and half European (not Jewish), then their different colored segments would be scattered across their entire set of chromosomes.

In this case, both of the tester’s parents are mixed – European Jewish (green) and Western Europe (blue.) We know both parents are admixed from the same two populations because in some locations, both parents contributed blue (Western Europe), and in other locations, both contributed Jewish (green) segments.

Both MyHeritage and Ancestry provide a secondary tool that’s connected to ethnicity, but different and generally in more recent times.

Ancestry’s DNA Communities

While your ethnicity may not point to anything terribly exciting in terms of endogamy, Genetic Communities might. Ancestry says that a DNA Community is a group of people who share DNA because their relatives recently lived in the same place at the same time, and that communities are much smaller than ethnicity regions and reach back only about 50-300 years.

Based on the ancestors’ locations in the trees of me and my matches, Ancestry has determined that I’m connected to two communities. In my case, the blue group is clearly my father’s line. The orange group could be either parent, or even a combination of both.

My endogamous Brethren could be showing up in Maryland, Pennsylvania, and Ohio, but it’s uncertain, in part, because my father’s ancestral lines are found in Virginia, West Virginia, and Maryland too.

These aren’t useful for me, but they may be more useful for fully endogamous people, especially in conjunction with ethnicity.

My Acadian cousin’s European ethnicity isn’t informative.

However, viewing his DNA Communities puts his French heritage into perspective, especially combined with his match surnames.

I wrote about DNA Communities when it was introduced with the name Genetic Communities, here.

MyHeritage’s Genetic Groups

MyHeritage also provides a similar feature that shows where my matches’ ancestors lived in the same locations as mine.

One difference, though, is that testers can adjust their ethnicity results confidence level from high, above, to low, below where one of my Genetic Groups overlaps my ethnicity in the Netherlands.

You can also sort your matches by Genetic Groups.

The results show you not only who is in the group, but how many of your matches are in that group too, which provides perspective.

I wrote about Genetic Groups, here.

Next, let’s look at how endogamy affects your matches.

Matches

The number of matches that a person has who is from an entirely endogamous community and a person with no endogamy may be quite different.

FamilyTreeDNA provides a Family Matching feature that triangulates your matches and assigns them to your paternal or maternal side by using known matches that you have linked to their profile cards in your tree. You must link people for the Family Matching feature known as “bucketing” to be enabled.

The people you link are then processed for shared matches on the same chromosome segment(s). Triangulated individuals are then deposited in your maternal, paternal, and both buckets.

Obviously, your two parents are the best people to link, but if they haven’t tested (or uploaded their DNA file from another vendor) and you have other known relatives, link them using the Family Tree tab at the top of your personal page.

I uploaded my Ancestry V4 kit to use as an example for linking. Let’s pretend that’s my sister. If I had not already linked my Ancestry V4 kit to “my sister’s” profile card, I’d want to do that and link other known individuals the same way. Just drag and drop the match to the correct profile card.

Note that a full or half sibling will be listed as such at FamilyTreeDNA, but an identical twin will show as a potential parent/child match to you. You’re much more likely to find a parent than an identical twin, but just be aware.

I’ve created a table of FamilyTreeDNA bucketed match results, by category, comparing the number of matches in endogamous categories with non-endogamous.

Total Matches Maternal Matches Paternal Matches Both % Both % DNA Unassigned
100% Jewish 34,637 11,329 10,416 4,806 13.9 23.3
100% Jewish 32,973 10,700 9,858 4,606 14 23.7
100% Jewish 32,255 9,060 10,970 3,892 12 25.8
75% Jewish 24,232 11,846 Only mother linked Only mother linked Only mother linked
100% Acadian 8093 3826 2299 1062 13 11
100% Acadian 7828 3763 1825 923 11.8 17
Not Endogamous 6760 3845 1909 13 0.19 14.5
Not Endogamous 7723 1470 3317 6 0.08 38
100% Native American 1,115 Unlinked Unlinked Unlinked
100% Native American 885 290 Unknown Can’t calculate without at least one link on both sides

The 100% Jewish, Acadian, and Not Endogamous testers both have linked their parents, so their matches, if valid (meaning not identical by chance, which I discussed here,) will match them plus one or the other parent.

One person is 75% Jewish and has only linked their Jewish mother.

The Native people have not tested their parents, and the first Native person has not linked anyone in their tree. The second Native person has only linked a few maternal matches, but their mother has not tested. They are seeking their father.

It’s very difficult to find people who are fully Native as testers. Furthermore, Native people are under-sampled. If anyone knows of fully Native (or other endogamous) people who have tested and linked their parents or known relatives in their trees, and will allow me to use their total match numbers anonymously, please let me know.

As you can see, Jewish, Acadian, and Native people are 100% endogamous, but many more Jewish people than Native people have tested, so you CAN’T judge endogamy by the total number of matches alone.

In fact, in order:

  • Fully Jewish testers have about 4-5 times as many matches as the Acadian and Non-endogamous testers
  • Acadian and Non-endogamous testers have about 5-6 times as many matches as the Native American testers
  • Fully Jewish people have about 30 times more matches than the Native American testers

If a person’s endogamy with a particular population is only on their maternal or paternal side, they won’t have a significant number of people related to both sides, meaning few people will fall into the “Both” bucket. People that will always be found in the ”Both” bucket are full siblings and their descendants, along with descendants of the tester, assuming their match is linked to their profiles in the tester’s tree.

In the case of our Jewish testers, you can easily see that the “Both” bucket is very high. The Acadians are also higher than one would reasonably expect without endogamy. A non-endogamous person might have a few matches on both sides, assuming the parents are not related to each other.

A high number of “Both” matches is a very good indicator of endogamy within the same population on both parents’ sides.

The percentage of people who are assigned to the “Both” bucket is between 11% and 14% in the endogamous groups, and less than 1% in the non-endogamous group, so statistically not relevant.

As demonstrated by the Native people compared to the Jewish testers, the total number of matches can be deceiving.

However, being related to both parents, as indicated by the “Both” bucket, unless you have pedigree collapse, is a good indicator of endogamy.

Of course, if you don’t know who your relatives are, you can’t link them in your tree, so this type of “hunt” won’t generally help people seeking their close family members.

However, you may notice that you’re matching people PLUS both of their parents. If that’s the case, start asking questions of those matches about their heritage.

A very high number of total matches, as compared to non-endogamous people, combined with some other hints might well point to Jewish heritage.

I included the % DNA Unassigned category because this category, when both parents are linked, is the percentage of matches by chance, meaning the match doesn’t match either of the tester’s parents. All of the people with people listed in “Both” categories have linked both of their parents, not just maternal and paternal relatives.

Matching Location at MyHeritage

MyHeritage provides a matching function by location. Please note that it’s the location of the tester, but that may still be quite useful.

The locations are shown in the most-matches to least-matches order. Clicking on the location shows the people who match you who are from that location. This would be the most useful in situations where recent immigration has occurred. In my case, my great-grandfather from the Netherlands arrived in the 1860s, and my German ancestors arrived in the 1850s. Neither of those groups are endogamous, though, unless it would be on a village level.

AutoClusters

Let’s shift to Genetic Affairs, a third-party tool available to everyone.

Using their AutoCluster function, Genetic Affairs clusters your matches together who match both each other and you.

This is an example of the first few clusters in my AutoCluster. You can see that I have several colored clusters of various sizes, but none are huge.

Compare that to the following endogamous cluster, sample courtesy of EJ Blom at Genetic Affairs.

If your AutoCluster at Genetic Affairs looks something like this, a huge orange blob in the upper left hand corner, you’re dealing with endogamy.

Please also note that the size of your cluster is also a function of both the number of testers and the match threshold you select. I always begin by using the defaults. I wrote about using Genetic Affairs, here.

If you tested at or transferred to MyHeritage, they too license AutoClusters, but have optimized the algorithm to tease out endogamous matches so that their Jewish customers, in particular, don’t wind up with a huge orange block of interrelated people.

You won’t see the “endogamy signature” huge cluster in the corner, so you’re less likely to be able to discern endogamy from a MyHeritage cluster alone.

The commonality between these Jewish clusters at MyHeritage is that they all tend to be rather uniform in size and small, with lots of grey connecting almost all the blocks.

Grey cells indicate people who match people in two colored groups. In other words, there is often no clear division in clusters between the mother’s side and the father’s side in Jewish clusters.

In non-endogamous situations, even if you can’t identify the parents, the clusters should still fall into two sides, meaning a group of clusters for each parent’s side that are not related to each other.

You can read more about Genetic Affairs clusters and their tools, here. DNAGedcom.com also provides a clustering tool.

Endogamous Relationships

Endogamous estimated relationships are sometimes high. Please note the word, “sometimes.”

Using the Shared cM Project tool relationship chart, here, at DNAPainter, people with heavy endogamy will discover that estimated relationships MAY be on the high side, or the relationships may, perhaps, be estimated too “close” in time. That’s especially true for more distant relationships, but surprisingly, it’s not always true. The randomness of inheritance still comes into play, and so do potential unknown relatives. Hence, the words “may” are bolded and underscored.

Unfortunately, it’s often stated as “conventional wisdom” that Jewish matches are “always” high, and first cousins appear as siblings. Let’s see what the actual data says.

At DNAPainter, you can either enter the amount of shared DNA (cM), or the percent of shared DNA, or just use the chart provided.

I’ve assembled a compilation of close relationships in kits that I have access to or from people who were generous enough to share their results for this article.

I’ve used Jewish results, which is a highly endogamous population, compared with non-endogamous testers.

The “Jewish Actual” column reports the total amount of shared DNA with that person. In other words, someone to their grandparent. The Average Range is the average plus the range from DNAPainter. The Percent Difference is the % difference between the actual number and the DNAPainter average.

You’ll see fully Jewish testers, at left, matching with their family members, and a Non-endogamous person, at right, matching with their same relative.

Relationship Jewish Actual Percent Difference than Average Average -Range Non-endogamous Actual Percent Difference than Average
Grandparent 2141 22 1754 (984-2482) 1742 <1 lower
Grandparent 1902 8.5 1754 (984-2482) 1973 12
Sibling 3039 16 2613 (1613-3488) 2515 3.5 lower
Sibling 2724 4 2613 (1613-3488) 2761 5.5
Half-Sibling 2184 24 1759 (1160-2436) 2127 21
Half-Sibling 2128 21 1759 (1160-2436) 2352 34
Aunt/Uncle 2066 18.5 1741 (1201-2282) 1849 6
Aunt/Uncle 2031 16.5 1741 (1201-2282) 2097 20
1C 1119 29 866 (396-1397) 959 11
1C 909 5 866 (396-1397) 789 9 lower
1C1R 514 19 433 (102-980) 467 8
1C1R 459 6 433 (102-980) 395 9 lower

These totals are from FamilyTreeDNA except one from GEDMatch (one Jewish Half-sibling).

Totals may vary by vendor, even when matching with the same person. 23andMe includes the X segments in the total cMs and also counts fully identical segments twice. MyHeritage imputation seems to err on the generous side.

However, in these dozen examples:

  • You can see that the Jewish actual amount of DNA shared is always more than the average in the estimate.
  • The red means the overage is more than 100 cM larger.
  • The percentage difference is probably more meaningful because 100 cM is a smaller percentage of a 1754 grandparent connection than compared to a 433 cM 1C1R.

However, you can’t tell anything about endogamy by just looking at any one sample, because:

  • Some of the Non-Endogamous matches are high too. That’s just the way of random inheritance.
  • All of the actual Jewish match numbers are within the published ranges, but on the high side.

Furthermore, it can get more complex.

Half Endogamous

I requested assistance from Jewish genealogy researchers, and a lovely lady, Sharon, reached out, compiled her segment information, and shared it with me, granting permission to share with you. A HUGE thank you to Sharon!

Sharon is half-Jewish via one parent, and her half-sibling is fully Jewish. Their half-sibling match to each other at Ancestry is 1756 cM with a longest segment of 164 cM.

How does Jewish matching vary if you’re half-Jewish versus fully Jewish? Let’s look at 21 people who match both Sharon and her fully Jewish half-sibling.

Sharon shared the differences in 21 known Jewish matches with her and her half-sibling. I’ve added the Relationship Estimate Range from DNAPainter and colorized the highest of the two matches in yellow. Bolding in the total cM column shows a value above the average range for that relationship.

Total Matching cMs is on the left, with Longest Segment on the right.

While this is clearly not a scientific study, it is a representative sample.

The fully Jewish sibling carries more Jewish DNA, which is available for other Jewish matches to match as a function of endogamy (identical by chance/population), so I would have expected the fully Jewish sibling to match most if not all Jewish testers at a higher level than the half-Jewish sibling.

However, that’s not universally what we see.

The fully Jewish sibling is not always the sibling with the highest number of matches to the other Jewish testers, although the half-Jewish tester has the larger “Longest Segment” more often than not.

Approximately two-thirds of the time (13/21), the fully Jewish person does have a higher total matching cM, but about one-third of the time (8/21), the half-Jewish sibling has a higher matching cM.

About one-fourth of the time (5/21), the fully Jewish sibling has the longest matching segment, and about two-thirds of the time (13/21), the half-Jewish sibling does. In three cases, or about 14% of the time, the longest segment is equal which may indicate that it’s the same segment.

Because of endogamy, Jewish matches are more likely to have:

  • Larger than average total cM for the specific relationship
  • More and smaller matching segments

However, as we have seen, neither of those are definitive, nor always true. Jewish matches and relationships are not always overestimated.

Ancestry and Timber

Please note that Ancestry downweights some matches by removing some segments using their Timber algorithm. Based on my matches and other accounts that I manage, Ancestry does not downweight in the 2-3rd cousin category, which is 90 cM and above, but they do begin downweighting in the 3-4th cousin category, below 90 cM, where my “Extended Family” category begins.

If you’ve tested at Ancestry, you can check for yourself.

By clicking on the amount of DNA you share with your match on your match list at Ancestry, shown above, you will be taken to another page where you will be able to view the unweighted shared DNA with that match, meaning the amount of DNA shared before the downweighting and removal of some segments, shown below.

Given the downweighting, and the information in the spreadsheet provided by Sharon, it doesn’t appear that any of those matches would have been in a category to be downweighted.

Therefore, for these and other close matches, Timber wouldn’t be a factor, but would potentially be in more distant matches.

Endogamous Segments

Endogamous matches tend to have smaller and more segments. Small amounts of matching DNA tend to skew the total DNA cM upwards.

How and why does this happen?

Ancestral DNA from further back in time tends to be broken into smaller segments.

Sometimes, especially in endogamous situations, two smaller segments, at one time separated from each other, manage to join back together again and form a match, but the match is only due to ancestral segments – not because of a recent ancestor.

Please note that different vendors have different minimum matching cM thresholds, so smaller matches may not be available at all vendors. Remember that factors like Timber and imputation can affect matching as well.

Let’s take a look at an example. I’ve created a chart where two ancestors have their blue and pink DNA broken into 4 cM segments.

They have children, a blue child and a pink child, and the two children, shown above, each inherited the same blue 4 cM segment and the same pink 4 cM segment from their respective parents. The other unlabeled pink and blue segments are not inherited by these two children, so those unlabeled segments are irrelevant in this example.

The parents may have had other children who inherited those same 4 cM labeled pink and blue segments as well, and if not, the parents’ siblings were probably passing at least some of the same DNA down to their descendants too.

The blue and pink children had children, and their children had children – for several generations.

Time passed, and their descendants became an endogamous community. Those pink and blue 4 cM segments may at some time be lost during recombination in the descendants of each of their children, shown by “Lost pink” and “Lost blue.”

However, because there is only a very limited amount of DNA within the endogamous community, their descendants may regain those same segments again from their “other parent” during recombination, downstream.

In each generation, the DNA of the descendant carrying the original blue or pink DNA segment is recombined with their partner. Given that the partners are both members of the same endogamous community, the two people may have the same pink and/or blue DNA segments. If one parent doesn’t carry the pink 4 cM segment, for example, their offspring may receive that ancestral pink segment from the other parent.

They could potentially, and sometimes do, receive that ancestral segment from both parents.

In our example, the descendants of the blue child, at left, lost the pink 4 cM segment in generation 3, but a few generations later, in generation 11, that descendant child inherited that same pink 4 cM segment from their other parent. Therefore, both the 4 cM blue and 4 cM pink segments are now available to be inherited by the descendants in that line. I’ve shown the opposite scenario in the generational inheritance at right where the blue segment is lost and regained.

Once rejoined, that pink and blue segment can be passed along together for generations.

The important part, though, is that once those two segments butt up against each other again during recombination, they aren’t just two separate 4 cM segments, but one segment that is 8 cM long – that is now equal to or above the vendors’ matching threshold.

This is why people descended from endogamous populations often have the following matching characteristics:

  • More matches
  • Many smaller segment matches
  • Their total cM is often broken into more, smaller segments

What does more, smaller segments, look like, exactly?

More, Smaller Segments

All of our vendors except Ancestry have a chromosome browser for their customers to compare their DNA to that of their matches visually.

Let’s take a look at some examples of what endogamous and non-endogamous matches look like.

For example, here’s a screen shot of a random Jewish second cousin match – 298 cM total, divided into 12 segments, with a longest segment of 58 cM,

A second Jewish 2C with 323 cM total, across 19 segments, with a 69 cM longest block.

A fully Acadian 2C match with 600 cM total, across 27 segments, with a longest segment of 69 cM.

A second Acadian 2C with 332 cM total, across 20 segments, with a longest segment of 42 cM.

Next, a non-endogamous 2C match with 217 cM, across 7 segments, with a longest segment of 72 cM.

Here’s another non-endogamous 2C example, with 169 shared cM, across 6 segments, with a longest segment of 70 cM.

Here’s the second cousin data in a summary table. The take-away from this is the proportion of total segments

Tester Population Total cM Longest Block Total Segments
Jewish 2C 298 58 12
Jewish 2C 323 69 19
Acadian 2C 600 69 27
Acadian 2C 332 42 20
Non-endogamous 2C 217 72 7
Non-endogamous 2C 169 70 6

You can see more examples and comparisons between Native American, Jewish and non-endogamous DNA individuals in the article, Concepts – Endogamy and DNA Segments.

I suspect that a savvy mathematician could predict endogamy based on longest block and total segment information.

Lara Diamond, a mathematician, who writes at Lara’s Jewnealogy might be up for this challenge. She just published compiled matching and segment information in her Ashkenazic Shared DNA Survey Results for those who are interested. You can also contribute to Laura’s data, here.

Endogamy, Segments, and Distant Relationships

While not relevant to searching for close relatives, heavily endogamous matches 3C and more distant, to quote one of my Jewish friends, “dissolve into a quagmire of endogamy and are exceedingly difficult to unravel.”

In my own Acadian endogamous line, I often simply have to label them “Acadian” because the DNA tracks back to so many ancestors in different lines. In other words, I can’t tell which ancestor the match is actually pointing to because the same DNA segments or segments is/are carried by several ancestors and their descendants due to founder effect.

The difference with the Acadians is that we can actually identify many or most of them, at least at some point in time. As my cousin, Paul LeBlanc, once said, if you’re related to one Acadian, you’re related to all Acadians. Then he proceeded to tell me that he and I are related 137 different ways. My head hurts!

It’s no wonder that endogamy is incredibly difficult beyond the first few generations when it turns into something like multi-colored jello soup.

“Are Your Parents Related?” Tool

There’s another tool that you can utilize to determine if your parents are related to each other.

To determine if your parents are related to each other, you need to know about ROH, or Runs of Homozygosity (ROH).

ROH means that the DNA on both strands or copies of the same chromosome is identical.

For a few locations in a row, ROH can easily happen just by chance, but the longer the segment, the less likely that commonality occurs simply by chance.

The good news is that you don’t need to know the identity of either of your parents. You don’t need either of your parent’s DNA tests – just your own. You’ll need to upload your DNA file to GEDmatch, which is free.

Click on “Are your parents related?”

GEDMatch analyzes your DNA to see if any of your DNA, above a reasonable matching threshold, is identical on both strands, indicating that you inherited the exact same DNA from both of your parents.

A legitimate match, meaning one that’s not by chance, will include many contiguous matching locations, generally a minimum of 500 SNPs or locations in a row. GEDmatch’s minimum threshold for identifying identical ancestral DNA (ROH) is 200 cM.

Here’s my result, including the graphic for the first two chromosomes. Notice the tiny green bars that show identical by chance tiny sliver segments.

I have no significant identical DNA, meaning my parents are not related to each other.

Next, let’s look at an endogamous example where there are small, completely identical segments across a person’s chromosome

This person’s Acadian parents are related to each other, but distantly.

Next, let’s look at a Jewish person’s results.

You’ll notice larger green matching ROH, but not over 200 contiguous SNPs and 7 cM.

GEDMatch reports that this Jewish person’s parents are probably not related within recent generations, but it’s clear that they do share DNA in common.

People whose parents are distantly related have relatively small, scattered matching segments. However, if you’re seeing larger ROH segments that would be large enough to match in a genealogical setting, meaning multiple greater than 7 cM and 500 SNPs,, you may be dealing with a different type of situation where cousins have married in recent generations. The larger the matching segments, generally, the closer in time.

Blogger Kitty Cooper wrote an article, here, about discovering that your parents are related at the first cousin level, and what their GEDMatch “Are Your Parents Related” results look like.

Let’s look for more clues.

Surnames

There MAY be an endogamy clue in the surnames of the people you match.

Viewing surnames is easier if you download your match list, which you can do at every vendor except Ancestry. I’m not referring to the segment data, but the information about your matches themselves.

I provided instructions in the recent article, How to Download Your DNA Match Lists and Segment Files, here.

If you suspect endogamy for any reason, look at your closest matches and see if there is a discernable trend in the surnames, or locations, or any commonality between your matches to each other.

For example, Jewish, Acadian, and Native surnames may be recognizable, as may locations.

You can evaluate in either or both of two ways:

  • The surnames of your closest matches. Closest matches listed first will be your default match order.
  • Your most frequently occurring surnames, minus extremely common names like Smith, Jones, etc., unless they are also in your closest matches. To utilize this type of matching, sort the spreadsheet in surname order and then scan or count the number of people with each surname.

Here are some examples from our testers.

Jewish – Closest surname matches.

  • Roth
  • Weiss
  • Goldman
  • Schonwald
  • Levi
  • Cohen
  • Slavin
  • Goodman
  • Sender
  • Trebatch

Acadian – Closest surname matches.

  • Bergeron
  • Hebert
  • Bergeron
  • Marcum
  • Muise
  • Legere
  • Gaudet
  • Perry
  • Verlander
  • Trombley

Native American – Closest surname matches.

  • Ortega
  • Begay
  • Valentine
  • Hayes
  • Montoya
  • Sun Bear
  • Martin
  • Tsosie
  • Chiquito
  • Yazzie

You may recognize these categories of surnames immediately.

If not, Google is your friend. Eliminate common surnames, then Google for a few together at a time and see what emerges.

The most unusual surnames are likely your best bets.

Projects

Another way to get some idea of what groups people with these surnames might belong to is to enter the surname in the FamilyTreeDNA surname search.

Go to the main FamilyTreeDNA page, but DO NOT sign on.

Scroll down until you see this image.

Type the surname into the search box. You’ll see how many people have tested with that surname, along with projects where project administrators have included that surname indicating that the project may be of interest to at least some people with that surname.

Here’s a portion of the project list for Cohen, a traditional Jewish surname.

These results are for Muise, an Acadian surname.

Clicking through to relevant surname projects, and potentially contacting the volunteer project administrator can go a very long way in helping you gather and sift information. Clearly, they have an interest in this topic.

For example, here’s the Muise surname in the Acadian AmerIndian project. Two great hints here – Acadian heritage and Halifax, Nova Scotia.

Repeat for the balance of surnames on your list to look for commonalities, including locations on the public project pages.

Locations

Some of the vendor match files include location information. Each person on your match list will have the opportunity at the vendor where they tested to include location information in a variety of ways, either for their ancestors or themselves.

Where possible, it’s easiest to sort or scan the download file for this type of information.

Ancestry does not provide or facilitate a match list, but you can still create your own for your closest 20 or 30 matches in a spreadsheet.

MyHeritage provides common surname and ancestral location information for every match. How cool is that!

Y DNA, Mitochondrial DNA, and Endogamy

Haplogroups for both Y and mitochondrial DNA can indicate and sometimes confirm endogamy. In other cases, the haplogroup won’t help, but the matches and their location information just might.

FamilyTreeDNA is the only vendor that provides Y DNA and mitochondrial DNA tests that include highly granular haplogroups along with matches and additional tools.

23andMe provides high-level haplogroups which may or may not be adequate to pinpoint a haplogroup that indicates endogamy.

Of course, only males carry Y DNA that tracks to the direct paternal (surname) line, but everyone carries their mother’s mitochondrial DNA that represents their mother’s mother’s mother’s, or direct matrilineal line.

Some haplogroups are known to be closely associated with particular ethnicities or populations, like Native Americans, Pacific Islanders, and some Jewish people.

Haplogroups reach back in time before genealogy and can give us a sense of community that’s not available by either looking in the mirror or through traditional records.

This Native American man is a member of high-level haplogroup Q-M242. However, some men who carry this haplogroup are not Native, but are of European or Middle Eastern origin.

I entered the haplogroup in the FamilyTreeDNA Discover tool, which I wrote about, here.

Checking the information about this haplogroup reveals that their common ancestor descended from an Asian man about 30,000 years ago.

The migration path in the Americans explains why this person would have an endogamous heritage.

Our tester would receive a much more refined haplogroup if he upgraded to the Big Y test at FamilyTreeDNA, which would remove all doubt.

However, even without additional testing, information about his matches at FamilyTreeDNA may be very illuminating.

The Q-M242 Native man’s Y DNA matches men with more granular haplogroups, shown above, at left. On the Haplogroup Origins report, you can see that these people have all selected the “US (Native American)” country option.

Another useful tool would be to check the public Y haplotree, here, and the public mitochondrial tree here, for self-reported ancestor location information for a specific haplogroup.

Here’s an example of mitochondrial haplogroup A2 and a few subclades on the public mitochondrial tree. You can see that the haplogroup is found in Mexico, the US (Native,) Canada, and many additional Caribbean, South, and Central American countries.

Of course, Y DNA and mitochondrial DNA (mtDNA) tell a laser-focused story of one specific line, each. The great news, if you’re seeking information about your mother or father, the Y is your father’s direct paternal (surname) line, and mitochondrial is your mother’s direct matrilineal line.

Y and mitochondrial DNA results combined with ethnicity, autosomal matching, and the wide range of other tools that open doors, you will be able to reveal a great deal of information about whether you have endogamous heritage or not – and if so, from where.

I’ve provided a resource for stepping through and interpreting your Y DNA results, here, and mitochondrial DNA, here.

Discover for Y DNA Only

If you’re a female, you may feel left out of Y DNA testing and what it can tell you about your heritage. However, there’s a back door.

You can utilize the Y DNA haplogroups of your closest autosomal matches at both FamilyTreeDNA and 23andMe to reveal information

Haplogroup information is available in the download files for both vendors, in addition to the Family Finder table view, below, at FamilyTreeDNA, or on your individual matches profile cards at both 23andMe and FamilyTreeDNA.

You can enter any Y DNA haplogroup in the FamilyTreeDNA Discover tool, here.

You’ll be treated to:

  • Your Haplogroup Story – how many testers have this haplogroup (so far), where the haplogroup is from, and the haplogroup’s age. In this case, the haplogroup was born in the Netherlands about 250 years ago, give or take 200 years. I know that it was 1806 or earlier based on the common ancestor of the men who tested.
  • Country Frequency – heat map of where the haplogroup is found in the world.
  • Notable Connections – famous and infamous (this haplogroup’s closest notable person is Leo Tolstoy).
  • Migration Map – migration path out of Africa and through the rest of the world.
  • Ancient Connections – ancient burials. His closest ancient match is from about 1000 years ago in Ukraine. Their shared ancestor lived about 2000 years ago.
  • Suggested Projects – based on the surname, projects that other matches have joined, and haplogroups.
  • Scientific Details – age estimates, confidence intervals, graphs, and the mutations that define this haplogroup.

I wrote about the Discover tool in the article, FamilyTreeDNA DISCOVER Launches – Including Y DNA Haplogroup Ages.

Endogamy Tools Summary Tables

Endogamy is a tough nut sometimes, especially if you’re starting from scratch. In order to make this topic a bit easier and to create a reference tool for you, I’ve created three summary tables.

  • Various endogamy-related tools available at each vendor which will or may assist with evaluating endogamy
  • Tools and their ability to detect endogamy in different groups
  • Tools best suited to assist people seeking information about unknown parents or grandparents

Summary of Endogamy Tools by Vendor

Please note that GEDMatch is not a DNA testing vendor, but they accept uploads and do have some tools that the testing vendors do not.

 Tool 23andMe Ancestry FamilyTreeDNA MyHeritage GEDMatch
Ethnicity Yes Yes Yes Yes Use the vendors
Ethnicity Painting Yes + segments Yes, limited Yes + segments Yes
Ethnicity Phasing Yes Partial Yes No
DNA Communities No Yes No No
Genetic Groups No No No Yes
Family Matching aka Bucketing No No Yes No
Chromosome Browser Yes No Yes Yes Yes
AutoClusters Through Genetic Affairs No Through Genetic Affairs Yes, included Yes, with subscription
Match List Download Yes, restricted # of matches No Yes Yes Yes
Projects No No Yes No
Y DNA High-level haplogroup only No Yes, full haplogroup with Big Y, matching, tools, Discover No
Mitochondrial DNA High-level haplogroup only No Yes, full haplogroup with mtFull, matching, tools No
Public Y Tree No No Yes No
Public Mito Tree No No Yes No
Discover Y DNA – public No No Yes No
ROH No No No No Yes

Summary of Endogamous Populations Identified by Each Tool

The following chart provides a guideline for which tools are useful for the following types of endogamous groups. Bolded tools require that both parents be descended from the same endogamous group, but several other tools give more definitive results with higher amounts of endogamy.

Y and mitochondrial DNA testing are not affected by admixture, autosomal DNA or anything from the “other” parent.

Tool Jewish Acadian Anabaptist Native Other/General
Ethnicity Yes No No Yes Pacific Islander
Ethnicity Painting Yes No No Yes Pacific Islander
Ethnicity Phasing Yes, if different No No Yes, if different Pacific Islander, if different
DNA Communities Yes Possibly Possibly Yes Pacific Islander
Genetic Groups Yes Possibly Possibly Yes Pacific Islander
Family Matching aka Bucketing Yes Yes Possibly Yes Pacific Islander
Chromosome Browser Possibly Possibly Yes, once segments or ancestors identified Possibly Pacific Islander, possibly
Total Matches Yes, compared to non-endogamous No No No No, unknown
AutoClusters Yes Yes Uncertain, probably Yes Pacific Islander
Estimated Relationships High Not always Sometimes No Sometimes Uncertain, probably
Relationship Range High Possibly, sometimes Possibly Possibly Possibly Pacific Islander, possibly
More, Smaller Segments Yes Yes Probably Yes Pacific Islander, probably
Parents Related Some but minimal Possibly Uncertain Probably similar to Jewish Uncertain, Possibly
Surnames Probably Probably Probably Not Possibly Possibly
Locations Possibly Probably Probably Not Probably Probably Pacific Islander
Projects Probably Probably Possibly Possibly Probably Pacific Islander
Y DNA Yes, often Yes, often No Yes Pacific Islander
Mitochondrial DNA Yes, often Sometimes No Yes Pacific Islander
Y public tree Probably not alone No No Yes Pacific Islander
MtDNA public tree Probably not No No Yes Pacific Islander
Y DNA Discover Yes Possibly Probably not, maybe projects Yes Pacific Islander

Summary of Endogamy Tools to Assist People Seeking Unknown Parents and Grandparents

This table provides a summary of when each of the various tools can be useful to:

  • People seeking unknown close relatives
  • People who already know who their close relatives are, but are seeking additional information or clues about their genealogy

I considered rating these on a 1 to 10 scale, but the relative usefulness of these tools is dependent on many factors, so different tools will be more or less useful to different people.

For example, ethnicity is very useful if someone is admixed from different populations, or even 100% of a specific endogamous population. It’s less useful if the tester is 100% European, regardless of whether they are seeking close relatives or not. Conversely, even “vanilla” ethnicity can be used to rule out majority or recent admixture with many populations.

Tools Unknown Close Relative Seekers Known Close Relatives – Enhance Genealogy
Ethnicity Yes, to identify or rule out populations Yes
Ethnicity Painting Yes, possibly, depending on population Yes, possibly, depending on population
Ethnicity Phasing Yes, possibly, depending on population Yes, possibly, depending on population
DNA Communities Yes, possibly, depending on population Yes, possibly, depending on population
Genetic Groups Possibly, depending on population Possibly, depending on population
Family Matching aka Bucketing Not if parents are entirely unknown, but yes if one parent is known Yes
Chromosome Browser Unlikely Yes
AutoClusters Yes Yes, especially at MyHeritage if Jewish
Estimated Relationships High Not No
Relationship Range High Not reliably No
More, Smaller Segments Unlikely Unlikely other than confirmation
Match List Download Yes Yes
Surnames Yes Yes
Locations Yes Yes
Projects Yes Yes
Y DNA Yes, males only, direct paternal line, identifies surname lineage Yes, males only, direct paternal line, identifies and correctly places surname lineage
Mitochondrial DNA Yes, both sexes, direct matrilineal line only Yes, both sexes, direct matrilineal line only
Public Y Tree Yes for locations Yes for locations
Public Mito Tree Yes for locations Yes for locations
Discover Y DNA Yes, for heritage information Yes, for heritage information
Parents Related – ROH Possibly Less useful

Acknowledgments

A HUGE thank you to several people who contributed images and information in order to provide accurate and expanded information on the topic of endogamy. Many did not want to be mentioned by name, but you know who you are!!!

If you have information to add, please post in the comments.

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FamilyTreeDNA DISCOVER™ Launches – Including Y DNA Haplogroup Ages

FamilyTreeDNA just released an amazing new group of public Y DNA tools.

Yes, a group of tools – not just one.

The new Discover tools, which you can access here, aren’t just for people who have tested at FamilyTreeDNA . You don’t need an account and it’s free for everyone. All you need is a Y DNA haplogroup – from any source.

I’m going to introduce each tool briefly because you’re going to want to run right over and try Discover for yourself. In fact, you might follow along with this article.

Y DNA Haplogroup Aging

The new Discover page provides seven beta tools, including Y DNA haplogroup aging.

Haplogroup aging is THE single most requested feature – and it’s here!

Discover also scales for mobile devices.

Free Beta Tool

Beta means that FamilyTreeDNA is seeking your feedback to determine which of these tools will be incorporated into their regular product, so expect a survey.

If you’d like changes or something additional, please let FamilyTreeDNA know via the survey, their support line, email or Chat function.

OK, let’s get started!

Enter Your Haplogroup

Enter your Y DNA haplogroup, or the haplogroup you’re interested in viewing.

If you’re a male who has tested with FamilyTreeDNA , sign on to your home page and locate your haplogroup badge at the lower right corner.

If you’re a female, you may be able to test a male relative or find a haplogroup relevant to your genealogy by visiting your surname group project page to locate the haplogroup for your ancestor.

I’ll use one of my genealogy lines as an example.

In this case, several Y DNA testers appear under my ancestor, James Crumley, in the Crumley DNA project.

Within this group of testers, we have two different Big Y haplogroups, and several estimated haplogroups from testers who have not upgraded to the Big Y.

If you’re a male who has tested at either 23andMe or LivingDNA, you can enter your Y DNA haplogroup from that source as well. Those vendors provide high-level haplogroups.

The great thing about the new Discover tool is that no matter what haplogroup you enter, there’s something for you to enjoy.

I’m going to use haplogroup I-FT272214, the haplogroup of my ancestor, James Crumley, confirmed through multiple descendants. His son John’s descendants carry haplogroup I-BY165368 in addition to I-FT272214, which is why there are two detailed haplogroups displayed for this grouping within the Crumley haplogroup project, in addition to the less-refined I-M223.

Getting Started

When you click on Discover, you’ll be asked to register briefly, agree to terms, and provide your email address.

Click “View my report” and your haplogroup report will appear.

Y DNA Haplogroup Report

For any haplogroup you enter, you’ll receive a haplogroup report that includes 7 separate pages, shown by tabs at the top of your report.

Click any image to enlarge

The first page you’ll see is the Haplogroup Report.

On the first page, you’ll find Haplogroup aging. The TMRCA (time to most recent common ancestor) is provided, plus more!

The report says that haplogroup I-FT272214 was “born,” meaning the mutation that defines this haplogroup, occurred about 300 years ago, plus or minus 150 years.

James Crumley was born about 1710. We know his sons carry haplogroup I-FT272214, but we don’t know when that mutation occurred because we don’t have upstream testers. We don’t know who his parents were.

Three hundred years before the birth of our Crumley tester would be about 1670, so roughly James Crumley’s father’s generation, which makes sense.

James’ son John’s descendants have an additional mutation, so that makes sense too. SNP mutations are known to occur approximately every 80 years, on average. Of course, you know what average means…may not fit any specific situation exactly.

The next upstream haplogroup is I-BY100549 which occurred roughly 500 years ago, plus or minus 150 years. (Hint – if you want to view a haplogroup report for this upstream haplogroup, just click on the haplogroup name.)

There are 5 SNP confirmed descendants of haplogroup I-FT272214 claiming origins in England, all of whom are in the Crumley DNA project.

Haplogroup descendants mean this haplogroup and any other haplogroups formed on the tree beneath this haplogroup.

Share

If you scroll down a bit, you can see the share button on each page. If you think this is fun, you can share through a variety of social media resources, email, or copy the link.

Sharing is a good way to get family members and others interested in both genealogy and genetic genealogy. Light the spark!

I’m going to be sharing with collaborative family genealogy groups on Facebook and Twitter. I can also share with people who may not be genealogists, but who will think these findings are interesting.

If you keep scrolling under the share button or click on “Discover More” you can order Y DNA tests if you’re a biological male and haven’t already taken one. The more refined your haplogroup, the more relevant your information will be on the Discover page as well as on your personal page.

Scrolling even further down provides information about methods and sources.

Country Frequency

The next tab is Country Frequency showing the locations where testers with this haplogroup indicate that their earliest known ancestors are found.

The Crumley haplogroup has only 5 people, which is less than 1% of the people with ancestors from England.

However, taking a look at haplogroup R-M222 with many more testers, we see something a bit different.

Ireland is where R-M222 is found most frequently. 17% of the men who report their ancestors are from Ireland belong to haplogroup R-M222.

Note that this percentage also includes haplogroups downstream of haplogroup R-M222.

Mousing over any other location provides that same information for that area as well.

Seeing where the ancestors of your haplogroup matches are from can be extremely informative. The more refined your haplogroup, the more useful these tools will be for you. Big Y testers will benefit the most.

Notable Connections

On the next page, you’ll discover which notable people have haplogroups either close to you…or maybe quite distant.

Your first Notable Connection will be the one closest to your haplogroup that FamilyTreeDNA was able to identify in their database. In some cases, the individual has tested, but in many cases, descendants of a common ancestor tested.

In this case, Bill Gates is our closest notable person. Our common haplogroup, meaning the intersection of Bill Gates’s haplogroup and my Crumley cousin’s haplogroup is I-L1195. The SNP mutation that defines haplogroup I-L1145 occurred about 4600 years ago. Both my Crumley cousin and Bill Gates descend from that man.

If you’re curious and want to learn more about your common haplogroup, remember, you can enter that haplogroup into the Discover tool. Kind of like genetic time travel. But let’s finish this one first.

Remember that CE means current era, or the number of years since the year “zero,” which doesn’t technically exist but functions as the beginning of the current era. Bill Gates was born in 1955 CE

BCE means “before current era,” meaning the number of years before the year “zero.” So 2600 BCE is approximately 4600 years ago.

Click through each dot for a fun look at who you’re “related to” and how distantly.

This tool is just for fun and reinforces the fact that at some level, we’re all related to each other.

Maybe you’re aware of more notables that could be added to the Discover pages.

Migration Map

The next tab provides brand spanking new migration maps that show the exodus of the various haplogroups out of Africa, through the Middle East, and in this case, into Europe.

Additionally, the little shovel icons show the ancient DNA sites that date to the haplogroup age for the haplogroup shown on the map, or younger. In our case, that’s haplogroup I-M223 (red arrow) that was formed about 16,000 years ago in Europe, near the red circle, at left. These haplogroup ancient sites (shovels) would all date to 16,000 years ago or younger, meaning they lived between 16,000 years ago and now.

Click to enlarge

By clicking on a shovel icon, more information is provided. It’s very interesting that I-L1145, the common haplogroup with Bill Gates is found in ancient DNA in Cardiff, Wales.

This is getting VERY interesting. Let’s look at the rest of the Ancient Connections.

Ancient Connections

Our closest Ancient Connection in time is Gen Scot 24 (so name in an academic paper) who lived in the Western Isles of Scotland.

These ancient connections are more likely cousins than direct ancestors, but of course, we can’t say for sure. We do know that the first man to develop haplogroup I-L126, about 2500 years ago, is an ancestor to both Gen Scot 24 and our Crumley ancestor.

Gen Scot 24 has been dated to 1445-1268 BCE which is about 3400 years ago, which could actually be older than the haplogroup age. Remember that both dating types are ranges, carbon dating is not 100% accurate, and ancient DNA can be difficult to sequence. Haplogroup ages are refined as more branches are discovered and the tree grows.

The convergence of these different technologies in a way that allows us to view the past in the context of our ancestors is truly amazing.

All of our Crumley cousin’s ancient relatives are found in Ireland or Scotland with the exception of the one found in Wales. I think, between this information and the haplogroup formation dates, it’s safe to say that our Crumley ancestors have been in either Scotland or Ireland for the past 4600 years, at least. And someone took a side trip to Wales, probably settled and died there.

Of course, now I need to research what was happening in Ireland and Scotland 4600 years ago because I know my ancestors were involved.

Suggested Projects

I’m EXTREMELY pleased to see suggested projects for this haplogroup based on which projects haplogroup members have joined.

You can click on any of the panels to read more about the project. Remember that not everyone joins a project because of their Y DNA line. Many projects accept people who are autosomally related or descend from the family through the mitochondrial line, the direct mother’s line.

Still, seeing the Crumley surname project would be a great “hint” all by itself if I didn’t already have that information.

Scientific Details

The Scientific Details page actually has three tabs.

The first tab is Age Estimate.

The Age Estimate tab provides more information about the haplogroup age or TMRCA (Time to Most Recent Common Ancestor) calculations. For haplogroup I-FT272214, the most likely creation date, meaning when the SNP occurred, is about 1709, which just happens to align well with the birth of James Crumley about 1710.

However, anyplace in the dark blue band would fall within a 68% confidence interval (CI). That would put the most likely years that the haplogroup-defining SNP mutation took place between 1634 and 1773. At the lower end of the frequency spectrum, there’s a 99% likelihood that the common ancestor was born between 1451 and 1874. That means we’re 99% certain that the haplogroup defining SNP occurred between those dates. The broader the date range, the more certain we can be that the results fall into that range.

The next page, Variants, provides the “normal” or ancestral variant and the derived or mutated variant or SNP (Single Nucleotide Polymorphism) in the position that defines haplogroup I-FT272214.

The third tab displays FamilyTreeDNA‘s public Y DNA Tree with this haplogroup highlighted. On the tree, we can see this haplogroup, downstream haplogroups as well as upstream, along with their country flags.

Your Personal Page

If you have already taken a DNA test at FamilyTreeDNA, you can find the new Discover tool conveniently located under “Additional Tests and Tools.”

If you are a male and haven’t yet tested, then you’ll want to order a Y DNA test or upgrade to the Big Y for the most refined haplogroup possible.

Big Y tests and testers are why the Y DNA tree now has more than 50,000 branches and 460,000 variants. Testing fuels growth and growth fuels new tools and possibilities for genealogists.

What Do You Think?

Do you like these tools?

What have you learned? Have you shared this with your family members? What did they have to say? Maybe we can get Uncle Charley interested after all!

Let me know how you’re using these tools and how they are helping you interpret your Y DNA results and assist your genealogy.

_____________________________________________________________

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Share the Love!

You’re always welcome to forward articles or links to friends and share on social media.

If you haven’t already subscribed (it’s free,) you can receive an email whenever I publish by clicking the “follow” button on the main blog page, here.

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I receive a small contribution when you click on some of the links to vendors in my articles. This does NOT increase the price you pay but helps me to keep the lights on and this informational blog free for everyone. Please click on the links in the articles or to the vendors below if you are purchasing products or DNA testing.

Thank you so much.

DNA Purchases and Free Uploads

Genealogy Products and Services

My Book

Genealogy Books

Genealogy Research