SAMN00004650

EXTERNAL
Sample
Accession
SAMN00004650
Alias
HG00132
Sex
Female
Center
NYGC
Description
Human 1000 genomes individual HG00132
Source publications
Y-DNA pathway
No haplogroup call for this sample.
mtDNA pathway chrM:13351G>C
From de-novo tree placement
  1. L1'2'3'4'5'6'7
    chrM:16181G>A
  2. L2'3'4'5'6'7
    chrM:12528G>A, chrM:15734C>T, chrM:16187C>T, chrM:2182A>G, chrM:2309C>T, chrM:6569G>A, chrM:7891T>C
  3. L2'3'4'6
    chrM:10111A>G, chrM:10233C>T, chrM:12929T>C, chrM:14724G>A, chrM:15610T>C, chrM:249A>T, chrM:8078T>C
  4. L3'4
    chrM:13073T>C, chrM:15701T>C, chrM:16174T>C, chrM:3017T>C, chrM:3527G>A, chrM:6679T>C, chrM:6944A>G
  5. L3
    chrM:193A>G, chrM:442A>G
  6. N
    chrM:10296C>T, chrM:14724A>G, chrM:8124G>A, chrM:8963C>T
  7. R
    chrM:15646T>C
  8. U
    chrM:10890A>G, chrM:11731A>G, chrM:11795G>A
  9. U5
    chrM:13040T>C, chrM:15693C>T
  10. U5a'b
    chrM:2620T>C, chrM:8900G>A
  11. U5a
    chrM:14216A>G, chrM:15679C>T
  12. U5a2
    chrM:15949G>A
  13. U5a2-C16294T
    chrM:15717C>T
  14. U5a2a1
    chrM:13250A>G, chrM:15537C>A
  15. chrM:13351G>C
    chrM:13351G>C
Origin
Sequencing & coverage

No sequencing data available.

Sequence data & files
Instrument: Illumina NovaSeq 6000 · Layout: PAIRED · Reads: 742558586 · Read length: 150 · Date: 2020-05-14
File Format Size Reference Aligner md5
HG00132.final.cram CRAM GRCh38 bwa mem 04bb6c14b69d6ccc859f50c17e86d1fc Download
Ancestry

No ancestry breakdown available.

Predicted phenotype and genetic-distance metrics are not yet available.