Variant Details

Variant: esv3586332

Internal ID

6973853

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:69530676..69537049	hg38	UCSC Ensembl
Inner	chr1:69530676..69537049	hg38	UCSC Ensembl
Outer	chr1:69530328..69537336	hg38	UCSC Ensembl
	chr1:69996359..70002732	hg19	UCSC Ensembl
Inner	chr1:69996359..70002732	hg19	UCSC Ensembl
Outer	chr1:69996011..70003019	hg19	UCSC Ensembl

Cytoband

1p31.1

Allele length

Assembly	Allele length
hg38	6374
hg19	6374

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv9961363, essv9961387, essv9961366, essv9961365, essv9961355, essv9961389, essv9961362, essv9961379, essv9961378, essv9961384, essv9961348, essv9961356, essv9961357, essv9961364, essv9961388, essv9961351, essv9961359, essv9961349, essv9961354, essv9961385, essv9961368, essv9961350, essv9961371, essv9961369, essv9961396, essv9961373, essv9961370, essv9961390, essv9961392, essv9961380, essv9961352, essv9961372, essv9961374, essv9961375, essv9961360, essv9961376, essv9961393, essv9961386, essv9961358, essv9961391, essv9961381, essv9961367, essv9961383, essv9961353, essv9961377, essv9961361, essv9961394, essv9961395, essv9961382

Samples

HG03096, HG02973, HG03175, HG03241, NA19377, HG03139, HG03577, HG03069, HG02769, NA19374, HG03452, HG02595, NA19904, HG02922, HG02505, HG03189, HG02623, HG03583, NA19921, NA19451, HG02716, HG02582, NA19913, NA19043, HG02887, NA18910, HG02878, HG01504, NA19740, HG03046, HG02585, NA20296, HG02813, HG02807, NA19108, NA18517, HG03437, HG02759, NA19037, HG02837, NA19360, HG03557, NA19475, NA19248, HG03112, HG02646, NA18505, HG02805, HG02760

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3586332

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	49
Observed Complex	0
Frequency	n/a