At Family Tree DNA, your Y DNA and full sequence mitochondrial matches display a column titled Genetic Distance. One of the most common questions I receive is how to interpret genetic distance.
Many people mistakenly assume that genetic distance is the number of generations to a common ancestor, but that is NOT AT ALL what genetic distance means.
Genetic distance is how many mutations difference the participant (you) has with that particular match. In other words, how many mismatches in your DNA compared with that person’s DNA.
White the concept is the same, Y DNA and mitochondrial DNA Genetic Distance function a little differently, so let’s look at them separately.
Y DNA Genetic Distance
I wrote about genetic distance as part of a larger article titled “Concepts – Y DNA Matching and Connecting with your Paternal Ancestor,” but I’m going to excerpt the genetic distance portion of that article here.
You’ll notice on the Y DNA matches page that the first column says “Genetic Distance.”
Looking at the example above, if this is your personal page, then you mismatch with Howard once, and Sam twice, etc.
Counting Genetic Distance
Genetic distance for Y DNA can be counted in different ways, and Family Tree DNA utilizes a combination of two scientific methods to provide the most accurate results. Let’s look at an example.
In the methodology known as the Step-Wise Mutation Model, each difference is counted as 1 step, because the mutation that caused the difference happened in one mutation event.
So, if marker 393 has mutated from 12 to 13, the difference is 1, so there is one difference and if that is the only mutation between these two men, the total genetic distance would be 1.
However, if marker 390 mutated from 24 to 26, the difference is 2, because those mutations most likely occurred in two different steps – in other words marker 390 had a mutation two different times, perhaps once in each man’s line. Therefore, the total genetic distance for these two men, combining both markers and with all of their other markers matching, would be 3.
Easy – right? You know this is too easy!
Some markers don’t play nice and tend to mutate more than one step at a time, sometimes creating additional marker locations as well. They’re kind of like a copy machine on steroids. These are known as multi-copy (or palindromic) markers and have more than one value listed for each marker. In fact, marker 464 typically has 4 different values shown, but can have several more.
The multiple mutations shown for those types of multi-copy markers tend to occur in one step, so they are counted as one event for that marker as a whole, no matter how much math difference is found between the values. This calculation method is called the Infinite Alleles Mutation Model.
Because marker 464 is calculated using the infinite alleles model, even though there are two differences, the calculation only notes that there IS a difference, and counts that difference as having occurred in one step, counting only as 1 in genetic distance.
However, if one man also has one or more extra copies of the marker, shown below as 464e and 464f, that is counted as one additional genetic distance step, regardless of the number of additional copies of the marker, and regardless of the values of those copies.
With markers 464e and 464f, which person 2 carries and person 1 does not, the difference is 17 and the generational difference is 1, for each marker, but since the copy event likely happened at one time, it’s considered a mutational difference or genetic distance of only 1, not 34 or 2. Therefore, in our example, the total genetic distance for these men is now 5, not 8 or 38.
In our last example, a deletion has occurred, which sometimes happens at marker location 425. When a deletion occurs, all of the DNA at that location is permanently deleted, or omitted, between father and son, and the value is 0. Once gone, that DNA has no avenue to ever return, so forever more, the descendants of that man show a value of zero at marker 425.
In this deletion example, even though the mathematical difference is 12, the event happened at once, so the genetic distance for a deletion is counted as 1. The total genetic distance for these two men now is 6.
In essence, the Total Genetic Distance is a mathematical calculation of how many times mutations happened between the lines of these two men since their common ancestor, whether that common ancestor is known or not.
Family Tree DNA provides a the TIP calculator which helps estimate the time to a common ancestor using a proprietary algorithm that includes individuals marker mutation rates. You can read more about this in the Y DNA Concepts article or in the TIP article.
Please note that on July 26, 2016 Family Tree DNA introduced changes in how the genetic distance is calculated for some markers to be less restrictive. You can read about the changes here.
Mitochondrial DNA Genetic Distance is a bit different. In order to be shown as a match, you must be an exact match in the HVR1 and HVR2 regions, so there is no genetic distance shown, because there are no mutations allowed.
At the full sequence level, you are allowed 4 or fewer mismatches to be considered a match.
Genetic distance means how many mismatches you have to another person when comparing your 16,569 mitochondrial locations to theirs. The full sequence test tests all of those locations.
Of course, in general, fewer mismatches mean you are more closely related than to someone with more mismatches. I said generally, because I have seen a situation where a mutation occurred between mother and child, meaning that individual had a genetic distance of 1 when compared to their mother, along with anyone who matched their mother exactly. Clearly, they are far more closely related to their mother than to their mother’s matches.
One of the most common questions I receive about genetic distance is how to convert genetic distance to time – meaning how long ago am I related to someone who has a genetic distance of 1 or 2, for example.
The answer is that it depends and it varies widely, very widely. I know, I hate the “it depends” answer too.
Turning to the Family Tree DNA Learning Center, we find the following information:
- Matching on HVR1 means that you have a 50% chance of sharing a common maternal ancestor within the last fifty-two generations. That is about 1,300 years.
- Matching on HVR1 and HVR2 means that you have a 50% chance of sharing a common maternal ancestor within the last twenty-eight generations. That is about 700 years.
- Matching exactly on the Mitochondrial DNA Full Sequence test brings your matches into more recent times. It means that you have a 50% chance of sharing a common maternal ancestor within the last 5 generations. That is about 125 years.
I think the full sequence estimate is overly generous. I seldom find identifiable matches, and I do have my genealogy back more than 5 generations on my mitochondrial line and so do many of my clients.
My 4 times great-grandmother, or 6 generations distant from me (counting my mother as generation 1), Elisabetha Mehlheimer, was found living in Goppmansbuhl, Germany when she gave birth to her daughter in 1823. This puts Elisabetha’s birth around 1800, or possibly earlier, very probably in the same village in Germany. German church records compulsively identify people who aren’t residents, and even residents who originally came from another location.
Part of my mitochondrial full sequence matches are shown below.
Looking at my 13 exact matches, it becomes obvious very quickly that my matches aren’t from Germany, they are primarily from Scandinavia. Not at all what I expected. I created this chart to view the match locations. I have omitted anyone who did not provide either location or oldest ancestor information. Fortunately, Scandinavians are very good about participating fully in DNA testing and by and large, they want to get the most out of their results. The way to do that, of course is to include as much information as possible so that we can all benefit by sharing and collaboration.
|Match||Genetic Distance||Location||Birth Year of Most Distant Ancestor|
|Anastasia||1||Russia above Georgia||1923|
|Marie M.||1||Bavaria, Germany||1836|
|Tomas||2||Probably Czech Republic||1880|
A quick look at my matches map shows the distribution of my matches more visually, although not everyone includes their matrilineal ancestor’s geographic information, so they don’t have pins on the map. In my case, I’m lucky because several people have included geographical information which makes the maps very useful. The white pin is where Elisabetha Mehlheimer lived. Red pins are exact matches, orange are one mutation difference and yellow are two.
I am very clearly not related to these individuals within 6 generations, and probably not for several more generations back in time. The one match from Germany is one mutation different, which certainly could mean that we share a common ancestor and her line had a mutation while mine line didn’t. Wurttemburg and Bavaria do share borders and are neighboring districts in southern Germany as illustrated by this 1855 map of Bavaria and Wurtemberg.
Unfortunately, there is no “rule of thumb” for mitochondrial DNA genetic distance relative to years and generations distant. In other words, there is no TIP calculator for mtDNA. I did some research some years ago attempting to quantify MRCA (most recent common ancestor) time and answer this very question, but the only research papers I was able to find referred to studies on penguins.
How Far is Far?
In some cases, I know that a common ancestor actually reached back hundreds to thousands of years. Of course, relationships in female lines are more difficult to “see” since the surname changes with every generation, historically. In Y DNA, you can look at the surname of the participant and determine immediately if there is a likelihood that you share a common paternal ancestor if the surname matches. Let’s look at some mitochondrial examples.
I recently had a client that matched her haplogroup assignment exactly, with no additional unusual mutations found as compared to the expected mitochondrial mutation profile. She had several exact matches. Her haplogroup? H7a2, which was formed about 2500 years ago, with a standard deviation of 2609, according to the supplemental date from the paper, “A “Copernican” Reassessment of the Human Mitochondrial DNA Tree from its Root” by Doron Behar, et al, published in The American Journal of Human Genetics, Volume 90, April 6, 2012. This means that H7a2 could have been formed anytime from recently to about 5000 years ago, with 2500 being the most likely and best fit.
Standard deviation, in this case, means the dates could be off that much in either direction, but the further from 2500, the less likely it is to be accurate.
Conversely, another recent client was haplogroup U2b formed roughly 30,000 years ago, with a standard deviation of 5,800 years. The client had 16 differences, which averages to about one mutation every 2,000 years. Is that what actually happened or did those mutations happen in fits and starts? We don’t know.
A last example is my own DNA with two relevant differences from my haplogroup profile, J1c2f, which was formed about 2,000 years ago with a standard deviation of 3,100 years. Technically, this means my haplogroup might not be formed yet (joke) since 2,000 years ago minus 3,100 years hasn’t happened yet. While that obviously can’t be true, the standard deviation is relevant in the other direction. In essence, what this says is that my haplogroup could be fairly young, probably is about 2000 years old, and could be as old as 5,100 years. Given the clustering, it’s likely that J1c2f was formed in Scandinavia and a few descendants, at some time, migrated into continental Europe and Russia.
By the way, the 315 “extra mutations” insertions are too unstable to be considered relevant. They are not included in the genetic distance count in your results.
At the other end of the spectrum, I know of one person who has a mutation between themselves and an aunt and a different mutation when compared with a sister. Furthermore, those mutations occurred in the HVR1 and HVR2 regions, meaning that these women don’t show as matches to each other until you get to the coding region where the full range of full sequence matches are shown and 4 mutations are allowed. This caused a bit of panic initially, but was perfectly legitimate and understandable once the actual results were compared. Is this rare? Absolutely. Is it possible? Absolutely.
As you can see, there just isn’t any good measure for mitochondrial DNA mutation timing. Mutations don’t happen on any time schedule, unfortunately.
I use genetic distance as a gauge for relative relatedness, no pun intended, and I keep in mind that I might actually be more closely related to someone with a slightly further genetic distance than an exact match.
While you can’t compare your actual results to matches online, you can contact your matches to compare actual results. In my case, I developed a branching tree mutation chart that showed that a group of the people in Sweden with one mutation difference actually all shared an additional mutation that I, and my exact matches, don’t have. In other words, this Swedish group forms a new branch of the tree and will likely, someday, be a new subhaplogroup of J1c2f.
Sometimes digging a little deeper reveals fascinating patterns that aren’t initially evident.
When working with genetic distance, look for patterns, not only in terms of geography, but in terms of matching mutations and grouping of individuals. Sometimes the combination of mutation patterns and geography can reveal information that could not be obtained any other way – and may lead you to your common ancestor, with or without a name.
For example, I know that my common ancestor with these people probably lived someplace in Scandinavia about 2000 years ago, based upon both the clustering and the branching. How my ancestor got to Germany is still a mystery, but one that might potentially be solved by looking at the history of the region where my known ancestor is found in 1800.
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