SAMN00014329
EXTERNALSample
- Accession
SAMN00014329- Alias
- HG01389
- Sex
- Male
- Center
- NYGC
- Description
- Human 1000 genomes individual HG01389
- Source publications
Y-DNA pathway
No haplogroup call for this sample.
mtDNA pathway
L1c3a1b
From de-novo tree placement
-
L1'2'3'4'5'6'7chrM:16181G>A
-
L1chrM:13212T>C, chrM:13601T>C, chrM:13983G>A, chrM:15716A>G, chrM:16181A>G, chrM:3089G>A, chrM:6478A>G, chrM:6812T>C
-
L1cchrM:10009G>A, chrM:12908A>G, chrM:13423T>A, chrM:14334C>T, chrM:15552G>A, chrM:15717C>T, chrM:15783C>T, chrM:16143C>T, chrM:16178C>A, chrM:16181G>C, chrM:16309G>A, chrM:5374A>G, chrM:5494T>C, chrM:7450G>A, chrM:8495A>G
-
L1c3chrM:10725C>T, chrM:14649A>G, chrM:15328T>C, chrM:15401C>T, chrM:16187C>T, chrM:5644T>A, chrM:6340G>A, chrM:6478A>G
-
L1c3achrM:11442C>T, chrM:15610T>C, chrM:15638A>G, chrM:15716A>G, chrM:5683G>A, chrM:6921G>A, chrM:7212G>A, chrM:9389G>A
-
L1c3a1chrM:15516T>C, chrM:2529A>G
-
L1c3a1bchrM:15778C>T, chrM:207A>G, chrM:8091T>C
Origin
Sequencing & coverage
No sequencing data available.
Sequence data & files
Instrument: Illumina NovaSeq 6000 ·
Layout: PAIRED ·
Reads: 700593002 ·
Read length: 150 ·
Date: 2020-05-14
| File | Format | Size | Reference | Aligner | md5 | |
|---|---|---|---|---|---|---|
| HG01389.final.cram | CRAM | — | GRCh38 | bwa mem | a9958cb5681a63b799b8ed5a01188757 | Download |
Ancestry
No ancestry breakdown available.
Predicted phenotype and genetic-distance metrics are not yet available.