DNA Results for Joe M. Newton

©Joe M. Newton

     

Y-Chromosome DNA analysis
Haplogroup: R1b1a2a1a1b3d2
(M207+ M173+ M343+ P25+ M269+ P312+ U152+ S47+)

Marker #
DYS#
Value
1
393
13
2
390
24
3
19 also known as 394
14
4
391
10
5
385a
11
6
385b
14
7
426
12
8
388
12
9
439
11
10
389i
13
11
392
15
12
389ii
29
13
458
18
14
459a
9
15
459b
10
16
455
10
17
454
12
18
447
25
19
437
15
20
448
19
21
449
30
22
454a
15
23
464b
15
24
464c
17
25
464d
17
26
460
11
27
Y-GATA-H4
11
28
YCAAIIa
20
29
YCAAIIb
23
30
456
15
31
607
15
32
576
18
33
570
18
34
CDYa
36
35
CDYb
39
36
442
12
37
438
12
38
461
13
39
462
11
40
GGAAT1B07
10
41
Y-GATA-A10
13
42
Y-GATA-C4
23
43
441
13
44
444
12
45
445
12
46
446
12
47
452
11
48
463
22
49
531
11
50
578
9
51
395S1a
15
52
395S1b
16
53
590
8
54
537
10
55
641
10
56
472
8
57
406S1
10
58
511
10
59
425
12
60
413a
23
61
413b
23
62
557
16
63
594
10
64
436
12
65
490
12
66
534
14
67
450
8
68
481
22
69
520
20
70
617
12
71
568
11
72
487
14
73
572
11
74
640
11
75
492
13
76
565
12

From a review of this DNA Y chromosome data you will see that DYS#392 has a value of 15. Current data extracted from the YHRD database in Berlin indicates that this value is rare and appears to have originated in the Eastern part of Germany or Northern part of Italy. The database shows the sequence to be most prevelant in the following four areas:

Greifswald, Germany (north coast of Germany)
Leipzig, Germany (just south of Berlin, Germany)
Liguria, Italy (on the border between Switersland and Italy)
Lombardy, Italy (north coast of Italy)

If you look at the map of Europe shown below, you will see a brown line that approximately connects these four areas. The southern end of this line stops on the coast of I taly (Liguria) while the northern end stops at the Baltic Sea town of Greufswald.

 

mtDNA analysis for Joe M. Newton

mtDNA Haplogroup K1a4

HVR1 differences from CRS     16224C, 16311C, 16519C

HVR2 differences from CRS     73G, 263G, 315.1C, 4 97T, 524.1C, 524.2A

Mitochondria are present in all human cells and contain their own DNA. Both males and females have this mtDNA, but only females pass it on to their offspring. Therefore, mtDNA is passed from mother to daughter along the female line without any influence from fathers. Therefore, since human mitochondrial DNA (mtDNA) is inherited only from the mother, it has distinct properties that make it an invaluable tool for genealogical and anthropological study. Because of this, the study of mtDNA is essentially the study of female genetic lines within human populations. Any mutations, of the base DNA sequence, are passed down to the children from the mother. Over time many mutations will occur, forming a detailed record of the maternal line in which it is a part. When this mtDNA record is studied in combination with other historical data, a particular mutation sequence can also be associated with a geographic area and population. This ability to connect mutations with places and populations has allowed researchers to constructed ancient migration patterns.

MtDNA analysis is performed by looking for both similarities and differences among individuals. In general, many DNA base pairs are analyzed and always includes the entire HVR-1 (HyperVariable Region 1) area, but many times also include the HVR-2 area. A base pair is a specific component of the DNA and is made of adenine (A) and guanine (G) or cytosine (C) and thymine (T). The HVR-1 area is mostly commonly analyzed because mutations occur more frequently in this region, which make the differentiation of specific lineages more easily. However, despite the fact that the HVR-1 region experiences mutations more frequently, the mutations do not occur often enough to determine whether two individuals are either closely or distantly related. Testing the HVR-2 area provides addition infomation that can assist in the determination of how closely two people are related.  In general, if two people share identical HVR-1 results, they have a 50% chance of being related in 56 generations (about 1,500 years).  However, with a match in both the HVR-1 and HVR-2 areas, the 50% chance of being ralated is reduced to 28 generation (about 700 years).  While the time frame for a common ancestor point is long, it is important to reme mber that if two people match, they do share a common female ancestor!

Research over the last decade suggests that all the maternal lines ultimately originate from “Mitochondrial Eve” approximately 140,000 years ago in Africa. However, my mtDNA sequence can be traced to a much more recent female who most likely lived in Northern Italy some 14,000 years ago.

Native Population Matches for Joe M. Newton

The data shown in the following table represents how my DNA matches Native Populations. These results are my Top 20 matches in a database of 808 native populations that have experienced minimal movement and admixture in modern history (approximately, the last 500 years). Individual matches do not necessarily indicate recent social or cultural affiliation with a particular ethnicity. Instead, the Native Population Match results identify populations where my DNA is most common, reflecting my deep ancestral origins. For people of multiple family origins, these matches can also identify populations where similar combinations of genetic material have taken place.

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Joe M. Newton