Mitotree Q&A for Everyone

I recently presented Mitotree Webinar – What It Is, How We Did It, and What Mitotree Means to You at Legacy Family Tree Webinars. It’s still free to view through June 13th, and after that, it’s available in the webinar library with a subscription. The 31-page syllabus is also a subscription feature.

Thank you to all 1000+ of you who attended and everyone else who has since watched the webinar – or will now.

We had a limited amount of time for Q&A at the end, so Geoff, our host, was kind enough to send me the list of questions from the Chat, and I’m doing the Q&A here. But keep in mind, please, that I’m assuming when I answer that you’ve watched the webinar or are familiar with how the new Mitotree and tools work.

That said, I think this Q&A can help everyone who is interested in mitochondrial DNA. Your genealogy gift from your mother and her female lineage.

Just a quick reminder that the mitochondrial DNA test tracks your direct matrilineal line only, meaning your mother’s mother’s mother’s line on up your tree until you run out of mothers. Of course, our goal is always to break through that brick wall.

This is a wonderful opportunity, because, unlike autosomal DNA, mitochondrial DNA is not admixed with the DNA of the other parent, so it’s a straight line look back directly up your mother’s female line.

Aha Moment!

Geoff said at the end that he had an aha moment during the webinar. Both males and females have mitochondrial DNA inherited from their mother, so we think of testing our own – but forget to obtain the mitochondrial DNA of our father. Testing your father’s mitochondrial DNA means obtaining your paternal grandmother’s mitochondrial DNA, so test your father to learn about his mother’s maternal line.

And it’s Father’s Day shortly.

Q&A

I’ve combined and summarized similar questions to make this short and sweet. Well, as short and sweet as I can make anything!

  • Can I benefit from Discover even if I don’t have a full sequence test?

You can benefit from the free FamilyTreeDNA Discover tool with any haplogroup, even a partial haplogroup. Be sure to click the down arrow and select mtDNA before entering the haplogroup if you’re using the public version.

However, to gain the most advantage from your test results and Discover, and to receive your closest matches, you need the full sequence test, called the mtFull, which you can purchase here. If you took one of the lower-level “Plus” tests, years ago, click here to sign in and upgrade or check your account to see if you have the full sequence test.

  • What benefits do I receive if I click through to Discover from my account versus using the public version of Discover?

Click any image to enlarge

If you click through to Discover directly from your FamilyTreeDNA account, you will receive features and additional information that are not available in the free, public version of Discover.

You’ll receive additional Notable Connections and up to 30 Ancient Connections based on how many are available and relevant for you.

You’ll also be able to view the Match Time tree, showing your matches, their earliest known ancestors, and where they fit in your haplogroup and haplotype cluster. In this example, two EKAs hinted at a common lineage, which turned out to be accurate after I did some digging.

I think the Match Time Tree is indispensable – the best thing since sliced bread!

The Scientific Details report is also customized for you with your Haplotype Cluster and your private variants.

  • Will a child and their mother always have the same haplogroup?

Yes, but if one of them has a mutation that the other doesn’t, or a heteroplasmy, they may be in a different haplotype cluster.

Also, they both need to have taken the full sequence test. Otherwise, the one who did not take the full sequence test will only have a partial haplogroup until they upgrade.

We will talk more about edge cases in Q&A on down the list.

Great question. Sign in to your account.

In the Maternal Line Ancestry section, which is mitochondrial DNA, check to see if both the Plus and Full boxes are pink. If so, you have taken both and you’ll have a new Mitotree haplogroup and haplotype cluster.

If the “Full” box is grey, you can either click there or at the top where it says “Add Ons and Upgrades” to upgrade to the full sequence test.

  • Why is it called the Million Mito Project? What were you counting?

When we first launched the project, we hoped for a million full sequence samples to build the initial tree. After removing duplicates, such as parent/child, partial sequence samples such as HVR1/2, unreliable samples from PhyloTree, and including FamilyTreeDNA  testers and academic samples, we had between one-third and half a million samples when we launched. The Mitotree and Discover are growing with new testers and groups of samples from archaeological studies, academic samples, and other publicly available resources, following quality analysis, of course.

  • Is there a way to confirm that I submitted an mtDNA to the Mito Tree project? I think I submitted my mom’s when you first started, but my husband recently tested, and I don’t remember if we opted him in at that time.

The science team at FamilyTreeDNA  is using all of the full sequence tests in the construction of the Mitotree, so you don’t need to do anything special.

  • Do or can haplotype F numbers (haplotype clusters) ever become haplogroups?

The answer is maybe. (I know – I’m sorry!)

If you have private variants in addition to your haplotype cluster, then yes, those are haplogroup seeds.

This is my result and I have no additional private variants left to use.

If you don’t have any private variants, or mutations, left over, then no, you won’t receive a new haplogroup for this reason. However, if for some reason the haplogroup splits upstream, you might receive a new haplogroup in the future due to that split.

In addition to the webinar, I wrote about haplotype clusters in the article, Mitochondrial DNA: What is a Haplotype Cluster and How Do I Find and Use Mine?

  • How can mitochondrial DNA and the Mitotree be useful for breaking down genealogy in various parts of the world?

There are two aspects to mitochondrial DNA testing.

The first is to connect genealogically, if possible. To do that, you’ll be paying attention to your matches EKAs (earliest known ancestors), their trees, and their locations. You may well need to do some genealogy digging and build out some trees for others.

The second aspect is to learn more about that lineage before you can connect genealogically. Where did they come from? Do they share a haplogroup with any Ancient Connections, and what cultures do they share? Where did they come from most recently in the world, and where do the breadcrumbs back in time lead?

I wrote about this in the article, New Mitotree Haplogroups and How to Utilize Them for Genealogy.

Sometimes, DNA testing of any type is simply a waiting game until the right person tests and matches you. That’s one reason it bothers me so much to see people “not recommend” mitochondrial DNA testing. We all need more testers so we can have more matches.

  • When will Globetrekker for mtDNA be available?

I don’t know and neither does the team. The Mitotree is still being refined. For example, we are adding thousands of samples to the tree right now from multiple locations around the world. I probably wouldn’t expect Globetrekker until the tree is officially out of Beta, and no, I don’t know when that will happen either. It’s difficult to know when you’re going to be “finished” with something that has never been done before.

While it’s not Globetrekker, you do have the Matches Map to work with, and the Migration Map in Discover, which also shows the locations of your Ancient Connections.

  • During the webinar, Roberta mentioned that her ancestor is German, but she discovered her ancestors were Scandinavian. Can you expand about the “event” that explained this unexpected discovery.

In my case, the church records for the tiny village where my ancestor lived in Germany begin right after the 30 Years’ War, which was incredibly destructive. Looking at Swedish troop movements in Germany, the army of Gustavus Adolphus of Sweden marched through the region with more than 18,000 soldiers. Women accompanied the baggage trains, providing essential, supportive roles and services to the soldiers and military campaign. I’ll never know positively, of course, but given that the majority of my full sequence matches are in Scandinavia, mostly Sweden, and not in Germany, it’s a reasonable hypothesis.

People often receive surprises in their results, and the history of the region plays a big role in the stories of our ancestors.

You don’t know what you don’t know, until you test and follow the paths ahd hints revealed.

  • Why do I have fewer matches in the HVR2 region than the HVR1 region?

Think of the mitochondria as a clock face.

The older (now obsolete) HVR1 test tested about 1000 locations, from about 11-noon and the HVR2/3 region tested another 1000 locations, from about noon-1 PM. The full sequence test tests the full 16,569 locations of the entire mitochondria.

Each level has its own match threshold. So, if you have one mutation at either the HVR1 or HVR2/3 level, combined, you are not considered a match. For example, you can match 10 people at the HVR1 level, and have a mutation in the HVR2 level that 4 people don’t share, so you’ll only match 6 people at the HVR2 level.

If you have one mutation in the HVR1 region, you won’t match anyone in either the HVR1 or HVR1/HVR2 regions.

At the full sequence level, you can have three mutation differences (GD 3) and still be considered a match.

So, the short answer is that you probably have a mutation that some of your matches at the HVR2 level don’t have.

In addition to matches on your Matches page, you will (probably) have haplogroup matches that aren’t on your match list, so check Discover for those.

  • I have HVR1/HVR2 matches, but none at the full sequence level. Why?

It’s possible that none of your matches have tested at that level.

You have no mutations in the HVR1/2 region, or you would not be a match. If your HVR1/2 matches have tested at the full sequence level, then you have more than 3 mutations difference in the coding region.

  • Why do I match people at the full sequence level but not HVR1/2?

The match threshold at the HVR1/2 level is 1, so if you have one mismatch, you’re not listed as a match. However, at the full sequence level, the GD (genetic distance) is 3 mismatches. This tells me you have a mismatch in the HVR1 region, which also precludes HVR2 matching, but less than 4 mutations total. Click on the little “i” button above each match level on the matches page.

  • Why don’t all of my matches show on the Match Time Tree?

Only full sequence matches can show on the Match Time Tree, because they are the only testers who can receive a full haplogroup.

  • How does a heteroplasmy interfere with mtDNA research?

Heteroplasmies, where someone carries two different nucleotides at the same location in different mitochondrial in their body, are both extremely fascinating and equally as frustrating.

Heteroplasmies can interfere with your matching because you might have a T nucleotide in a specific location, which matches the reference model, so no mutation – like 16362T. Your mother might have a C in that location, so T16362C, which is a mutation from T to C. Your aunt or sister might have both a T and a C, which means she is shown with letter Y, so 16362Y, which means she has more than 20% of both. All three of you probably have some of each, but it’s not “counted” as a heteroplasmy unless it’s over 20%.

The challenge is how to match these people with these different values accurately, and how heteroplasmies should “count” for matching.

I wrote about this in the article What is a Heteroplasmy and Why Do I Care?

Bottom line is this – if you are “by yourself” and have no matches, or you don’t match known relatives exactly, suspect a heteroplasmy. If you ask yourself, “What the heck is going on?” – rule out a heteroplasmy. Check out my article and this heteroplasmy article in the FamilyTreeDNA help center.

  • Someone asked about the X chromosome and may have been confusing it with mitochondrial DNA. The X chromosome is not the same as mitochondrial DNA.

The confusion stems from the fact that both are associated with inheritance from the maternal line. Everyone inherits their mitochondrial DNA from their mother. Men inherit their X chromosome ONLY from their mother, because their father gives them a Y chromosome, which makes them a male. Females inherit an X chromosome from both parents. And yes, there are medical exceptions, but those are unusual.

I wrote about this in the article, X Matching and Mitochondrial DNA is Not the Same Thing.

  • How do you determine the location of the last mutation? A tester and their aunt are from one country, and another man in the same haplogroup is from another country, but he has tested only the HVR1/HVR2 level.

There are really two answers here.

First, you can’t really compare your full sequence new Mitotree haplogroup with a partial haplogroup based on only the HVR1/2 test. Chances are very good that if he upgraded to a full sequence test, he would receive a more complete haplogroup, and one that might be near the tester’s haplogroup, but perhaps not the same.

For example, my full sequence haplogroup is J1c2f. I have matches with people who only tested at the HVR1/HVR2 level, but they can only be predicted to haplogroup J, with no subgroup, because they are missing about 14,000 locations that are included in the full sequence test.

Using the Discover Compare feature, comparing haplogroup J to J1c2f clearly shows that the mutations that define haplogroup J1c2f happened long after the mutation(s) that define haplogroup J.

You can use other Discover tools such as the Match Time Tree (if you click through from your account), the Time Tree, the Ancestral Path and the Classic Tree to see when the various haplogroups were born.

  • My mother took the full sequence test in 2016, so should I look for an upgrade now? She is deceased so can’t retest.

First, I’m sorry for your loss, but so glad you have her DNA tests.

The good news is that you ordered the full sequence right away, so you don’t need to worry about an upgrade failing later. In this case, there is no upgrade because the full sequence tests all 16,569 locations.

Additionally, had you needed an upgrade, or wanted to do a Family Finder test, for example, FamilyTreeDNA stores the DNA vials for future testing, so you could potentially run additional tests.

And lastly, since we’re talking mitochondrial DNA, which you inherit from your mother with no admixture from your father, your mtDNA should match hers exactly, so you could test in proxy for her, had she not already tested.

  • Has anything changed in Native American haplogroups?

Absolutely. About 75% of testers received a new haplogroup and that includes people with Native American matrilineal ancestors.

For example, my Native ancestor was haplogroup A2f1a, formed about 50 CE and is now A2f1a4-12092, formed about 1600 CE, so has moved 2 branches down the tree and about 1500 years closer. My ancestor was born about 1683. Her descendant has 58 full sequence matches, 22 in the same haplogroup, and 16 people in their haplotype cluster.

I’m so excited about this, because it helps provide clarity about her ancestors and where they were before she entered my genealogy by marrying a French settler.

  • Are mtDNA mutations the same or similar to autosomal SNPs?

A SNP is a single nucleotide polymorphism, which means a single variation in a specific location. So yes, a mutation is a change in a nucleotide at a genetic location in Y-DNA, autosomal DNA, or mitochondrial DNA.

  • Can we filter or sort our matches by haplotype on our match page?

Not yet. Generally, your closest matches appear at or near the top of your match list. Of course, you can use the Discover Match Time Tree and you can download your matches in a CSV file. (Instructions are further down in Q&A.)

  • Is there a way to make it more obvious that the EKA should be in their matrilineal line? There are so many men as EKAs!

So frustrating. The verbiage has been changed and maybe needs to be revised again, but of course, that doesn’t help with the people who have already entered males. We know males aren’t the source of mitochondrial DNA.

When I see males listed as an EKA, I send the match a pleasant note. I’m not sure they make the connection between what they entered and what is being displayed to their matches. If they have included or linked to a tree, I tell them who, in their tree, is their mtDNA EKA.

I’ve written about how to correctly add an Earliest Known Ancestor. I’ll update that article and publish again so that you can forward those instructions to people with no EKA, or male EKAs.

  • I love learning about my ancient connections. I have a new match due to the updates, who is from a neighboring area to my great-great-great-grandmother.

I love, love, LOVE Ancient Connections. They tell me who my ancestors were before I have any prayer of identifying them individually. Then I can read up on the culture from which they sprang.

I’ve also had two situations where Ancient Connections have been exceptionally useful.

One is an exact haplogroup match to my ancestor, and the burial was in a necropolis along the Roman road about 3-4 km outside the medieval “city” where my ancestor lived.

In a second case, there were two villages in different parts of the same country, hundreds of miles apart, and one burial from about 200 years before my ancestor lived was found about 10 km from one of those villages. While this isn’t conclusive, it’s certainly evidence.

  • What does the dashed line on the Time Tree mean?

Dashed lines on the time tree can mean two things.

The red dashed line, red arrow above, is the haplogroup formation date range and correlates to the dates at the top of Time Tree, not show in this screen shot. You can also read about those dates and how they are calculated on the Scientific Details tab in Discover.

The brown dashed lines, green arrow above, connect an ancient sample to its haplogroup, but the sample date is earlier than the estimated haplogroup.

At first this doesn’t make sense, until you realize that ancient samples are sometimes carbon dated, sometimes dated by proximity to something else, and sometimes dated based on the dates of the cemetery or cultural dig location.

Archaeological samples can also be contaminated, or have poor or low coverage. In other words, at this point in time, the samples are listed, but would need to be individually reviewed before shifting the haplogroup formation date. Haplogroup formation dates are based on present day testers.

  • A cousin and I have been mtDNA tested. What might be gained by testing our other six female cousins/10 or so male cousins?

Probably not much, so here’s how I would approach this.

I would test one cousin who descends from another daughter of the EKA, if possible. This helps to sift out if a haplogroup-defining mutation has occurred.

If you or that cousin has private variants left over after their haplotype cluster is formed,  testing a second person from that line may well results in a new haplogroup formation for that branch.

I absolutely would ask every single one of those cousins to take an autosomal test, however, because you never know what tools the future will bring, and we want to leverage every single segment of DNA that our ancestors carried. Testing cousins in the only way to find those.

  • In the Mitotree, I am grouped in a haplogroup that, according to the Mitotree Match Time Tree, branched off only about 200 years ago and has four mtDNA testers in it, including me. In fact, my earliest known maternal line ancestor I found using pen-and-paper genealogy was indeed born around 230 years ago and is also the known maternal ancestor for one of these three testers – confirming the Mitotree grouping is correct. But the other two matches in this haplogroup are completely unknown to me. Unfortunately, they do not have a tree online, and they did not respond to several messages. Is there any way to find out more about them using the new Mitotree tools?

First of all, this is great news. Having said that, I share your frustration. However, you’re a genealogist. Think of yourself as a sleuth.

I’d start by emailing them, but in this case, you already have. Tell them what you know from your line and ask if their line is from the same area? End with a question for them to answer. Share tidbits from Discover – like Ancient Connections maybe. Something to peak their interest.

Next, put on your sleiuh hat. I’d google their name and email address, and check Facebook and other social media sites. I’d check to see if they match me, or any cousins who have tested, on an autosomal test. If they do match autosomally, use shared matching and the matrix tool. If they are an autosomal match, I’d also check other testing sites to see if they have a tree there.

  • One webinar attendee is haplogroup H1bb7a+151 and is frustrated because they only have eight matches and don’t understand how to leverage this.

Of course, without knowing more, I can’t speak to what they have and have not done, and I certainly understand their frustration. However, in mitochondrial and Y-DNA, you really don’t want thousands of matches. It’s not autosomal. You want close, good matches, and that’s what the Mitotree plus haplotype clusters provide.

Your personal goals also make a lot of difference.

For me, I wanted to verify what I think I know – and received a surprise. I also want to go further back if possible. Then, I want to know the culture my ancestors came from.

First, step through every single one of Discover’s 13 tools and READ EVERY PAGE – not skim. These are chapters in your free book about your ancestor.

Their haplogroup was formed about 1200, so all of those matches will be since that time. The Ancient Connections tell me it’s probably British, maybe Irish – but they will see more from their account than I can see on the public version of Discover.

The Time Tree shows me one haplotype cluster, which is where the tester’s closest matches will probably be, barring a mutation or heteroplasmy.

Looking at the matches, e-mail people, look for common locations in their trees, and see if any of them are also autosomal matches using the Advanced Matching tool.

Looking at the 10 success story examples I used, one man was able to connect 19 of his matches into three groups by doing their genealogy for them. This doesn’t work for everyone, but it will never work if we don’t make the attempt.

  • An attendee would like to search on the Earliest Known Ancestor’s (EKA’s) name field.

I would like that too. You can search on surnames, but that’s often not terribly useful for mitochondrial DNA. The Match Time Tree shows the EKA for all full sequence testers.

In the upper right hand corner of your Matches page, there’s an “Export CSV” file link. Click there to download in a spreadsheet format. The EKA is a column in that file, along with both the new Mitotree haplogroup and haplotype F number, and it’s very easy to do a sort or text search from there.

  • Several questions about why people have so many more autosomal matches than either Y-DNA or mitochondrial.

There are several considerations.

First, autosomal testing became very popular, often based on ethnicity. There are many times more autosomal testers than there are either Y or mitochondrial.

Second, if you look back just six generations, you have 64 lineages. Y-DNA and mtDNA tests one line each and you don’t have to figure out which line. It also reaches back much further in time because it’s not admixed, so nothing washes out or rolls off in each generation like with autosomal.

Third, the Y-DNA and mitochondrial DNA tests are very specific and granular.

More is not necessarily better. You’re looking for refinement – and mitochondrial is just one line. No confusion. Think how happy you’d be if your autosomal matches weren’t all jumbled together and could be placed into 64 neat little baskets. Think how much time we spend sorting them out by shared matches and other criteria. Both Y-DNA and mitochondrial is already sorted out.

I’ve broken through several brick walls with unrecombined Y-DNA and mitochondrial DNA that could never be touched with autosomal – especially older lines where autosomal DNA is either gone or negligible.

  • You mentioned a Facebook group where I can ask questions about mitochondrial DNA?

The mitochondrial DNA Facebook group is the FamilyTreeDNA mtDNA Group, here.

  • To the webinar attendee who came to see me more than 20 years ago at Farmington Hills, Michigan, at one of my first, if not the first, genetic genealogy presentation – thank you!

Thank you for attending then when I really had no idea if ANYONE would come to hear about this new DNA “thing” for genealogy. I remember how nervous I was. And thank you for sticking around, continuing to research, and saying hello now!

Closing Comment

Mitochondrial DNA testing is different than autosomal, of course. It’s often the key to those females’ lines with seemingly insurmountable brick walls.

I attempt to collect the mitochondrial DNA of every ancestor. I trace “up the tree” to find people to test who descend from those ancestors through all women to the current generation, which can be males.

To find testers, I shop:

  • Autosomal matches at FamilyTreeDNA
  • Projects at FamilyTreeDNA
  • WikiTree
  • FamilySearch
  • Ancestry DNA matches
  • Ancestry Thrulines
  • Ancestry trees
  • MyHeritage DNA matches, where ther are a lot more European testers
  • MyHeritage Theories of Family Relativity
  • MyHeritage Cousin Finder
  • Relatives at RootsTech during the month before and after RootsTech when it’s available
  • Facebook Genealogy and family groups that appear relevant

When I find an appropriately descended person, I ask if they have already taken either the Y-DNA or mitochondrial DNA test, whichever one I’m searching for at that moment. If yes, hurray and I ask if they will share at least their haplogroup. If they haven’t tested, I tell them I’m offering a testing scholarship.

I will gladly explain the results if they will share them with me. Collaboration is key and a rising tide lifts all ships.

My mantra in all of this is, “You don’t know what you don’t know, and if you don’t test, you’ll never know.” I’ve missed testing opportunities that I desperately wish I hadn’t, so test your DNA and find testers to represent your ancestors.

I hope you enjoyed the webinar. It’s not too late to watch.

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DNAExplain Blog to be Preserved for Future Generations in the Library of Congress

Yes, indeed, this is definitely a red-letter event!!!

Not only is having my blog archived in the Library of Congress an incredible honor, but it solves a long-standing problem. Let’s start at the beginning.

In the Beginning…

I started this blog, www.dna-explained.com, also www.dnaexplain.com, for three primary reasons:

  • To educate the public, specifically genetic genealogists, about effectively using DNA for genealogy.
  • To share my own and other relevant vendor and non-vendor research and advancements in the field.
  • To provide a timeline and cumulative progressive history of this emerging field, recorded as it occurred. Essentially an industry diary.

My first blog article was published in July of 2012. The direct-to-consumer genetics industry was about 12 years old at that time. Today, the industry is roughly 23 years old and my blog is approaching its 11th anniversary. I’ve covered nearly half of the life of the genetic genealogy industry.

I recently crossed the threshold of 1600 published articles which equates to about 2.5 articles each week. Those articles total over 4 million words, or more than 15,000 pages of text, plus 20,000 images. That’s about half the size of the Encyclopedia Brittanica. That level of writing and publishing is almost a full-time job, alone, without anything else. Yet, I need to perform the research and do the work to create the content of each article. Not to mention the rest of my activities that pay the bills.

Anyone who writes, specifically, those who write to publish regularly, such as a blog, know that blogging isn’t exactly easy and requires an incredible amount of investmented time. The majority of blogs are abandoned shortly after creation. I fully understand why. You have to love both the process of writing and the subject – and be willing to contribute. Not to mention monitoring and approving the more than 50,000 comments and such.

As you know, this blog is free. I don’t charge for a subscription. I don’t accept paid content, guest articles or write articles for pay. I do have affiliate links at the bottom, but consider those cumulative purchases equivalent to buying me a cup of coffee. (Thank you to those who purchase through those links.)

There is some recurring financial investment in blogging too, but the biggest commitment, by far, is time. Hours and days that can’t be spent elsewhere, like on genealogy, for example – which leads me to my 52 Ancestors articles.

52 Ancestors

Of those slightly more than 1600 articles, 465 are in my 52 Ancestors series. I’m “blaming,” or crediting, Amy Johnson Crow for this, because in January of 2014, she challenged genealogists to write something about one ancestor a week and share or publish it someplace, somehow. I really liked that idea, and came to discover that focusing on one ancestor at a time, not a couple, and not their parents or children, allowed me to live with them for a bit and view their life through their eyes alone. So many times we know very little about our ancestor’s lives, and even less about the women. Interweaving Y-DNA and mitochondrial DNA results and matches, relationships and the history of what was happening around them provides an invaluable tool to connect with their lives.

I wasn’t sure I could maintain that one article per week pace, but I wanted to try. The 52 Ancestors challenge was just for one year, right? I could stop anytime, right? But how would I share? I didn’t really think any of you would be interested in MY ancestors, so I very nearly didn’t publish these stories on my blog. I’m INCREDIBLY glad that I did, because I use both genealogy and genetic tools at multiple vendors to confirm those ancestors, to find and identify their descendants, and to break though next-generation brick walls. Plus, I’ve discovered innumerable wonderful cousins!

Having committed, I jumped into 52 Ancestors with both feet and immediately addressed a very long-standing mystery about my father’s missing son. What I didn’t expect to happen was for you, my readers, to help solve it, but you did!!! Two weeks later, Lee was identified, had a name and a history! Wow we were off and running at breakneck speed. To this day, the 52 Ancestors articles remain some of my favorites, along with the process of bringing those ancestors back to life, even if just through words.

Sometimes I don’t write about ancestors specifically, but memorable events in our lifetimes that we’ve shared, like the 1969 moon landing, Y2K and more recently, the anniversary of the space shuttle Challenger explosion. Don’t you wish someone had written or journaled about contemporary milestones in our ancestor’s lives? What I wouldn’t give for that!

Preservation and Perpetuity

One of the reasons I write about my ancestors and genetic genealogy more broadly is because I very much want to share with other researchers, now and in the future.

In some cases, I’m the contributor, but often others contribute invaluable information to me. I firmly believe that a rising tide lifts all ships.

My goal is twofold:

  • To educate others and share methodologies so they can find and confirm their ancestors.
  • To complete the painting of my ancestor’s lives, or as much as I can in my lifetime.

Both of these are foundations upon which others can build.

A few years ago, I began to be concerned with preservation in perpetuity. How might I preserve those stories and the rest of my blog? I realize that in time, the technical aspects of my blog articles will be dated, but the educational basics remain firm. Better research methodologies will be developed. New information, both paper trail and genetic, will, hopefully, be unearthed about my ancestors, but I want the information I’ve provided to remain accessible over time.

I’ve been a technologist long enough to know that nothing is forever. Web sites disappear every day. The Internet Archive is wonderful, but it too may go poof, not to mention that you need to know the website url to access the archived website.

I reached out to WordPress, my blogging platform a few years ago. I asked if I could pay in advance for a “permanent” website, but they said that after payment stopped for the domain name and my subscription for the “non-free” platform, that my articles would revert to a free WordPress site “forever.” That means the url would change. Of course, none of the original links would work, and its value would be much dimished given that the articles would not appear in search engines. Furthermore, “forever” in technology days could be very short indeed.

Resources like FamilySearch aren’t meant for publications like my blog, and neither is WikiTree, especially “someday” after the blog link is no longer valid. I’ve posted links to articles on my blog on the ancestors’ profiles at WikiTree and in my personal trees at MyHeritage and Ancestry, but once the link is gone, effectively, so is the information.

I could copy the articles to word/pdf documents and attach those files to the trees, but we really don’t know what will and will not have longevity in today’s technical genealogical environment. Plus, I don’t want my articles behind a paywall anyplace, especially since I’ve made them available for free.

However, the Library of Congress has now solved that quandary for me and I’m both elated and honored.

The Invitation  

In the crazy days leading up to RootsTech, a gem of an email landed in my inbox. It was supposedly the Library of Congress (LOC) requesting to archive this blog and make this website available for all perpetuity as part of a collection of historically and culturally significant websites designated for preservation.

That’s quite a compliment.

I wasn’t quite sure I believed it. In fact, I was pretty sure that I didn’t.

Of course, the first thing I thought was that these were really brilliant scammers.

I contacted the LOC and discovered that this email was, indeed, genuine. I was both shocked and humbled.

To Whom It May Concern:

The United States Library of Congress requests permission to include your website in the Local History and Genealogy Web Archive, which is part of a larger collection of historically and culturally significant websites that have been designated for preservation. The following URL has been selected for archiving: https://dna-explained.com/.

The Library hopes that you share its vision of preserving digital content and making it available to current and future generations of researchers. As the internet has become an increasingly important and influential part of our lives, we believe the historical record would be incomplete if websites like yours are not preserved and made a part of it. We also believe that expanding access to the Library’s collections is one of the best ways we can increase opportunities for education and scholarship around the world. Please provide the Library with permission to archive your website and provide public access to archived versions of your website by filling out the form available here: <link redacted.>

With your permission, the Library of Congress or its agent will engage in the collection of content from your website at regular intervals over time. In order to properly archive the above URL, we may archive other portions of the website and public content that your page links to on third party sites such as social media platforms. In addition to the aforementioned collection, archived content from your website may be added to other relevant collections in the future. This content would be available to researchers only at Library facilities or by special arrangement, unless you additionally grant the Library permission for the content to become more broadly available through hosting on the Library’s public website, which would be done no sooner than one year after it was collected. For more information on the web archiving process, please read our frequently asked questions.

We encourage you to learn more about the Library’s Web Archiving program and explore our collections to see examples of how we archive websites. If you have any questions, comments, or recommendations concerning the archiving of your website, please email the Library’s Web Archiving Team at webcapture@loc.gov.

Thank you.

Library of Congress Web Archiving Team

It would be an understatement to say I was incredibly excited. There were no balloons or jubilant noisemakers though, and the cats were unimpressed as I clicked and agreed for my collective body of work to succeed me “forever.” Who knew milestones like this were so quiet, with only me winking to Mom and Dad who I’m positive were watching and silently cheering!

Here’s the confirmation of my acceptance.

So, in another hundred years, just like I can search for, say, Estes photos from a century or more ago at the Library of Congress, people living four or five generations in the future will be able to search for and read about the very early days of genetic genealogy and find those ancestor stories. They will also be able to learn something about the time in which we live today.

I can stop worrying about more than a decade’s worth of work disappearing after I join my ancestors, hopefully to obtain the answers that have eluded me here.

I’m incredibly, incredibly humbled and grateful to the Library of Congress for this amazing opportunity to contribute to our collective heritage. Thanks to each and every one of you for joining me on our journey into the history books.

_____________________________________________________________

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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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Mitochondrial DNA Resources – Everything You Need to Know

Mitochondrial DNA Resources

Recently, I wrote a multi-part series about mitochondrial DNA – start to finish – everything you need to know.

I’ve assembled several articles in one place, and I’ll add any new articles here as well.

Please feel free to share this resource or any of the links to individual articles with friends, genealogy groups or on social media.

What the Difference Between Mitochondrial and Other Types of DNA?

Mitochondrial DNA is inherited directly from your matrilineal line, only, meaning your mother’s mother’s mother’s mother – on up your family tree until you run out of direct line mothers that you’ve identified. The great news is even if you don’t know the identities of those people in your tree, you carry their mitochondrial DNA which can help identify them.

Here’s a short article about the different kinds of DNA that can be used for genealogy.

Why Mitochondrial DNA?

Let’s start out with why someone might want to test their mitochondrial DNA.

After you purchase a DNA test, swab, return the kit and when the lab finishes processing your test, you’ll receive your results on your personal page at FamilyTreeDNA, the only company that tests mitochondrial DNA at the full sequence level and provides matching with tens of thousands of other testers.

What About Those Results?

People want to understand how to use all of the different information provided to testers. These articles provide a step-by-step primer.

Mitochondrial DNA personal page update

Sign in to your Family Tree DNA account and use these articles as a guideline to step through your results on your personal page.

We begin with an overview. What is mitochondrial DNA, how it is inherited and why is it useful for genealogy?

Next, we look at your results and decode what all the numbers mean. It’s easy, really!

Our ancestors lived in clans, and our mitochondrial DNA has its own versions of clans too – called haplogroups. Your full haplogroup can be very informative.

Sometimes there’s more than meets the eye. Here are my own tips and techniques for more than doubling the usefulness of your matches.

You’ll want to wring every possible advantage out of your tests, so be sure to join relevant projects and use them to their fullest extent.

Do you know how to utilize advanced matching? It’s a very powerful tool. If not, you will after these articles.

Mitochondrial DNA Information for Everyone

FamilyTreeDNA maintains an extensive public mitochondrial DNA tree, complete with countries of origin for all branches. You don’t need to have tested to enjoy the public tree.

However, if you have tested, take a look to see where the earliest known ancestors of your haplogroup matches are located based on the country flags.

Mitochondrial resources haplotree

These are mine. Where are yours?

What Can Mitochondrial DNA Do for You?

Some people mistakenly think that mitochondrial DNA isn’t useful for genealogy. I’m here to testify that it’s not only useful, it’s amazing! Here are three stories from my own genealogy about how I’ve used mitochondrial DNA to learn more about my ancestors and in some cases, break right through brick walls.

It’s not only your own mitochondrial DNA that’s important, but other family members too.

My cousin tested her mitochondrial DNA to discover that her direct matrilineal ancestor was Native American, much to her surprise. The great news is that her ancestor is my ancestor too!

Searching for Native American Ancestors?

If you’re searching for Native American or particular ancestors, mitochondrial DNA can tell you specifically if your mitochondrial DNA, or that of your ancestors (if you test a direct matrilineal descendant,) is Native, African, European, Jewish or Asian. Furthermore, your matches provide clues as to what country your ancestor might be from and sometimes which regions too.

Did you know that people from different parts of the world have distinctive haplogroups?

You can discover your ancestors’ origins through their mitochondrial DNA.

You can even utilize autosomal segment information to track back in time to the ancestor you seek. Then you can obtain that ancestor’s mitochondrial DNA by selectively testing their descendants or finding people who have already tested that descend from that ancestor. Here’s how.

You never know what you’re going to discover when you test your mitochondrial DNA. I discovered that although my earliest known matrilineal ancestor is found in Germany, her ancestors were from Scandinavia. My cousin discovered that our common ancestor is Mi’kmaq.

What secrets will your mitochondrial DNA reveal?

You can test or upgrade your mitochondrial DNA by clicking here.

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Disclosure

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 Transfers

Genealogy Services

Genealogy Research

Norwegian Cultural Gems – Burial Practices, Cemeteries, Heritage Clothing and Family Traditions

I must say, I’ve never had such an enjoyable airport bus ride before. Unfortunately, based on my flight time, I was boarding a bus at my Oslo hotel before 5 AM for the hour ride to the airport. Oslo was deserted.

I sat in the front seat, as I tend to suffer from motion sickness. The bus had one, count ‘em, one other rider. I intended to sleep.

The driver must have been bored out of his mind, as he pulled up to stop after stop with no one waiting. He asked me what brought me to Oslo.

“A genealogy conference,” I replied, and he told me that his aunt had done their family genealogy and was watching some “special” on her computer all weekend. Yep, you guessed it, she was watching the MyHeritage LIVE conference.

As we drove through the Norwegian night, he explained a great deal about their family customs and in particular, funerary culture.

Burial Traditions

His family had lived in Oslo for generations, as long as the records reached back in time. They used to own land in the city center, being wealthy merchants and traders. As such, they bought a “row” of 10 cemetery plots generations ago.

I asked where the current generation would be buried because, given how long his family had owned their row, surely it was full by now.

That’s when my education began.

Triple-Bunk Burials

First, he told me that they bury people 3 deep, stacked one on top of the other.

“Oh,” I said, “that’s interesting,” – wondering silently about how deep that bottom person needs to be planted. I asked about concrete vaults and he said they don’t use them in Norway. He asked why we’d want to. I’ve wondered the same thing myself, many times.

Of course, I’m pondering the logistics of how this triple-bunking works, but they’ve had generations to perfect the details.

Then, I wondered whose name is on the gravestone? Or is there a gravestone? He explained, “With each new person buried, another name gets added to the stone.”

He told me that his parents are divorced, but when his mother’s “time comes” they will bury her in the family “row,” but not on top of Dad. Neither one of them would like that. “No, no!” he reiterated, shaking his head vigorously. I’m sure there’s a story there.

Next, I asked when their 30 “slots” would be full and what happens then?

Recycled Graves 

“Well,” he replied, “then we dig up everyone and start all over, reusing the entire grave.”

What? How would they know that the top person was “ready.”

He indicated that they have special probes and they poke around in the grave to be sure the casket and body are sufficiently decayed.

Ok, that took a moment to sink in. I was trying desperately not to see visuals of this at 5 in the morning and couldn’t help but think of bad puns.

Hmm, OK, that makes sense – but that would take a long time. I looked into decay rates when I was considering exhuming my father and discovered that after 50 years, the skin has started to decay – but then, that’s with embalming. Maybe these people weren’t embalmed.

I asked how long they wait before using the entire gravesite again.

Expecting to hear an answer something like 50 or 100 years, I was shocked when he said “10 years.”

So I asked, “What do they do with the bones?”

“There aren’t any bones.”

I decided to spare him the morbidity of the decay rate study I read and the archaeology digs I’ve been a part of. Clearly, there are some bones that survive for hundreds of years.

“What if there are bones?”

“I don’t know.”

“Do they have ossuaries in Norway for any remaining bones to continue returning to dust?”

“What’s an ossuary?”

Thinking that maybe translation was an issue, since ossuary isn’t a common word, I explained that an ossuary is a little house in the cemetery for the bones to be housed in, similar in size to a shed, while they finished decaying. 

“No, he said, nothing like that.”

The Honor of Payment

He paused for a few minutes to pull over at the next stop, then said that the honor of paying goes to the oldest son.

“Paying? For what?”

“For the graves?”

“For maintenance?”

“No, the cemetery takes care of mowing the grass. It’s so that no one else can be buried in the grave.”

“But your family bought the land?”

“Yes, but if we don’t pay every year, someone else will be buried in the grave.”

“How soon?”

“Whenever we no longer pay, unless the entire plot is full, and then it’s as soon as the top grave is decayed so they can dig them all up and reuse the spot.”

“What happens to the headstones if someone else is buried on top that isn’t a family member?”

“The old headstone is removed.”

“Thrown away?”

“No, moved to a different location in the cemetery. The person who keeps the books can tell you where it is.”

“So your ancestors could be in graves 1 and 2 of the triple-bunk graves, then no one pays the annual bill so a non-family-member is buried in the top grave. Your family stone is removed and only the top person has a stone, but your ancestors are still actually buried there, even though the stone has been removed? What happens then?”

“If the family of the third (top) person pays the annual fee, the grave won’t be used for at least 10 years, and maybe not after that if they continue to pay.”

“When they stop paying?”

“Then all 3 graves get dug up and someone else is buried there.”

Cremation

“Are people cremated in Norway?”

“Sometimes. It’s not very popular, but it’s gaining popularity now. Sometimes they create small rows in cemeteries, or you can bury the cremated remains in your own row if you have one. But it’s not traditional.”

“Do they cremate people here because of cost?”

“I don’t know. A full funeral with a visitation costs about 2500.” (US)

“Wow, that’s at least 4 times less expensive than in the US.”

He paused as we rounded a corner.

Gallows Hill

“See that church in the distance? That’s called Gallows Hill. In the dark ages, when someone was hung, everyone from the city came and sat on the hill, looking up, watching the top where the person would be hung, near the church. The actual place of execution is gone today, but it’s still called Gallows Hill.”

I love old cities.

We drove on, stopping at another stop with no people waiting. He had to wait a minute or two, just in case, so he pointed to the right, into the inky night.

Grave Candles

“See those tiny lights flickering over there?”

I squinted.

“Yes.”

“Those are candles in the cemetery, on the graves.”

“Candles? It’s 5 AM.”

“Yes, people leave them to honor their family and ancestors and almost anytime you can see candles burning.”

I saw quite a few, and it was a weekday early morning.

“At Christmas, people decorate the graves and everyone lights candles. The cemetery is lit up beautifully and if it snows, it’s incredibly scenic with an otherworldly glow. I can’t explain it.”

You can read more about candles in Norway, here. Norwegians love candles. You view photos here.

“How do the flames keep from being extinguished?”

“There are special kinds of long-burning candles, but some people just use regular candles. There’s no electricity in the cemetery, of course.”

“Does your family do that?”

“Yes. Several of my siblings and myself don’t believe in religion, but we still all go to church together as a family on Christmas Day. We wear our traditional Norwegian folk costumes. Afterwards, we all go to the cemetery to visit the ancestors. For those people we knew, we light candles, and sometimes we light candles on all of the 10 spaces.”

Birthday Celebrations in the Cemetery

“When it’s warm, we go on their birthday and have coffee and crackers (cookies) and sit round, laugh and reminisce fondly. It’s a celebration. When it’s cold, we don’t stay so long.”

“So, it’s a happy time. No tears?”

“Well, it can sometimes be sad too, but we are together. Often we stay a couple hours and talk about the person, remembering their life. My grandfather, he was the best, most honorable man on earth. I miss him but I like spending time at his grave.”

I reflected on this lovely custom for a few minutes. 

“I like that your culture views it as an honor to be selected to pay for the plots, and not a burden.”

“We have other similar traditions.”

Inheritance of Heirlooms

“In my family, a hand-made clock always goes to the eldest son before he is age 30. It has never been owned by a woman. That clock, when my parents were getting divorced, it was sad.”

“Sad?”

“Yes, sad. We knew because it lost 8 minutes every night. When the divorce was over, it recovered and never lost time anymore. 

Specific antique chairs go to the second eldest child, whether male or female.  That’s me!” and he smiles broadly.

“Another heirloom goes to the oldest living family member. In my case, when my Dad dies, that will be my aunt, if she is still living then.

An ax gets passed to someone, although who gets it is always a surprise, along with the story of who owned the ax and the legend of the ax. It was used by my ancestor to clear the trees for Oslo.”

“Was he a Viking?”

“Maybe!”

He smiles.

Traditional Clothing

“Sometimes our traditional costumes get passed down too. They are very, very expensive, costing several thousands of dollars.” (US)

So, I thought, funerals are cheap by comparison and traditional costumes (called Bunads) are more expensive than funerals, beginning at about $3000 (US).

“Tell me about the costumes.”

“Every person in Norway is either supposed to purchase a traditional costume, their parents purchase the costume, or it’s made or bequeathed to you by a family member. Each village and region has their own style, and you’re supposed to make a traditional style that connects you with where your ancestors were from. There is traditional jewelry that goes along with them too.

See that store over there? They specialize in traditional costumes, but the costumes are very expensive no matter where you purchase them.”

“When do you wear them?”

“I ordered mine for a friend’s wedding, because I needed it quickly. No time to have it made. I also grew a celebration mustache for having my niece baptized last weekend. I wore my costume then too. We wear the costumes for special occasions like that, National days of celebration plus holidays sometimes. When we want to dress up. It’s our finest, most proud clothing and reflects the unique culture of where our ancestors were born, no matter where we live today. Some people can identify your family place of birth by looking at your costume. It’s our way of wearing our heritage.”

Here’s an example of a girl from the fjord near Hardanger, with beautiful traditional Hardanger embroidery on her apron.

Arvind (அரவிந்தன்) – Self-photographed

If you’d like to view some lovely Norwegian heritage clothes, click here and then click on the front, back and side views.

Culture of Tradition 

I so enjoyed his family stories and was so grateful that he chose to enlighten a stranger on his bus in the middle of the night.

These traditions may not be shared by all families, but certainly, they provide a perspective of life in Scandinavia in a family that still values and cherishes their ancestors and family customs.

And yes, I did ask if he had DNA tested and he said that his brother and aunt had both tested, and they were mostly Scandinavian. He was wondering why they were ethnically anything else, which is highly ironic since many of us have been trying to figure out for years why we are Scandinavian.

I hope you’ve enjoyed my bus ride. I surely did!

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Disclosure

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 Transfers

Genealogy Services

Genealogy Research