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"Danish Demes"
Lineages and Results of mtDNA Testing for a Regional Danish DNA Project
Haplogroup V — "Clan Velda"
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H (11) J (1) K (2) T (3) U (2) V (2)
Mitochondrial DNA Haplogroup V, popularly known as, "Clan Velda," is most closely related to Haplogroup H, "Clan Helena."  Hg V appears to have originated about 16-17,000 years ago in Spain making it the youngest of the mtDNA haplogroups.  Clans Helena and Velda may be the only ones to have evolved after humans reached Europe (i.e., after leaving the Middle East).  Hg H is the most common haplogroup in Europe, being represented in about half the population, while Hg V is the rarest, being represented in only about 4% of Europeans.  Hg V is found thinly throughout Europe, but is most common among the Basques of northern Spain and the Saami people of Finland.  Whit Athey has an excellent discussion of Haplogroup V on his web site.  We have two project members who are Hg V.

In the trivia department, a matrilineal descendant of Benjamin FRANKLIN's maternal grandmother has been mtDNA tested, and she is Haplogroup V.

The Cambridge Reference Sequence (CRS) is arbitrarily designated as the standard against which all mtDNA sequences are compared, and subject test results are expressed as differences from the CRS.  The CRS happens to be negative for the 519C mutation, which is otherwise very common, so the majority of tested individuals will have this mutation listed in the HVR1 region.
In the table below, a darkened empty cell means the test was not ordered.  All HVR1 marker designations begin with "16___"; so, to save space and improve readability, I've dropped the 16 in the tables.  With regard to results, a letter in red indicates a mutation (a base has changed); a letter in green indicates a new base has been inserted; a minus sign (-) indicates a base has been lost.
With regard to lineages, given names and patronymics are shown as Initial Caps, while surnames are shown in ALL-CAPS (these are the womens' maiden names, not their married names).
Your project admin recommends uploading your mtDNA results to MitoSearch.org, which can be done at your FTDNA member page (on the "mtDNA Matches" tab).

Deme 1
Kit # MitoSearch
User ID
Differences from Cambridge Referece Sequence Known Lineage
HVR1 HVR2
63974 Z2UFK 298C 72C, 204C, 263G, 309.1C, 309.2C*, 315.1C Dau9, Dau8, Dau7, Ulrikke Abeline BENTSEN6, Mariane Bentine BENDTSEN5, Karen Rasmusdatter4, Karen Jørgensdatter3, Sidsel Nielsdatter2, Kirsten Olisdatter1 — of Skamstrup Sogn, Tuse Herred, Holbæk Amt, DK
In the FTDNA database, this individual has hundreds of HVR1 matches, but just one HVR1+HVR2 match.
*Our subject was tested at a second laboratory (Genetic Ancestors), which came up with the same results as FTDNA, except for a second insertion of C at location 309.

Deme 2
Kit # MitoSearch
UserID
Differences from Cambridge Reference Sequence Known Lineage
HVR1 HVR2
63184 - 298C 72C, 263G, 309.1C, 315.1C Pvt8, Pvt7, Borghild Irene HANSEN6, Olga Marie Kirstine HANSEN5, Ane LARSEN4, Maren Kirtine Hansdatter3, Ane Larsdatter2, Anne Kirstine Rasmusdatter1 — of Fjelsted, Vends Herred, Odense Amt, DK
In the FTDNA database, this individual has over 400 matches in his HVR1 region and over 50 matches in his combined HVR1+HVR2 regions.


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