Variant Details

Variant: esv3617634

Internal ID

7004519

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr8:73433227..73436283	hg38	UCSC Ensembl
	chr8:74345462..74348518	hg19	UCSC Ensembl

Cytoband

8q21.11

Allele length

Assembly	Allele length
hg38	3057
hg19	3057

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv13225833, essv13225820, essv13225819, essv13225813, essv13225838, essv13225854, essv13225847, essv13225809, essv13225830, essv13225844, essv13225845, essv13225837, essv13225817, essv13225842, essv13225818, essv13225810, essv13225850, essv13225853, essv13225815, essv13225848, essv13225851, essv13225828, essv13225812, essv13225824, essv13225811, essv13225814, essv13225832, essv13225835, essv13225802, essv13225816, essv13225823, essv13225841, essv13225806, essv13225840, essv13225843, essv13225849, essv13225829, essv13225821, essv13225825, essv13225846, essv13225834, essv13225826, essv13225822, essv13225831, essv13225803, essv13225836, essv13225852, essv13225839, essv13225808, essv13225827, essv13225807, essv13225804, essv13225805

Samples

HG03096, HG02944, NA18861, HG03175, HG03300, NA18917, NA20321, NA19092, NA19443, NA20320, NA19307, NA18923, HG02549, NA18916, HG03246, HG03105, NA19138, HG02922, HG03189, HG02571, HG03073, NA19027, HG03169, HG03120, HG02977, HG03054, NA19984, HG03547, HG01882, HG02470, NA18907, HG03451, HG03391, NA18523, NA19095, HG02586, HG01988, HG03109, HG01896, NA19206, HG02557, NA19108, HG03367, NA19310, HG01342, NA19143, HG03112, NA19223, HG03279, HG01914, NA19146, NA19312, HG03271

Known Genes

STAU2, STAU2-AS1

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3617634

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	53
Observed Complex	0
Frequency	n/a