Variant Details

Variant: esv3643752

Internal ID

6683822

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr19:14804503..14812143	hg38	UCSC Ensembl
Inner	chr19:14804503..14812143	hg38	UCSC Ensembl
Outer	chr19:14804176..14812522	hg38	UCSC Ensembl
	chr19:14915315..14922955	hg19	UCSC Ensembl
Inner	chr19:14915315..14922955	hg19	UCSC Ensembl
Outer	chr19:14914988..14923334	hg19	UCSC Ensembl

Cytoband

19p13.12

Allele length

Assembly	Allele length
hg38	7641
hg19	7641

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15997521, essv15997483, essv15997498, essv15997481, essv15997512, essv15997519, essv15997500, essv15997504, essv15997499, essv15997501, essv15997522, essv15997478, essv15997516, essv15997493, essv15997497, essv15997515, essv15997485, essv15997503, essv15997513, essv15997517, essv15997480, essv15997490, essv15997506, essv15997510, essv15997482, essv15997494, essv15997487, essv15997484, essv15997509, essv15997488, essv15997479, essv15997511, essv15997502, essv15997492, essv15997514, essv15997486, essv15997523, essv15997489, essv15997507, essv15997491, essv15997505, essv15997496, essv15997508, essv15997520, essv15997477, essv15997518, essv15997495

Samples

HG02628, NA19204, HG02433, HG03057, HG03130, NA19393, HG02624, HG02769, HG03385, HG02541, HG02620, HG03460, HG02703, HG02573, NA18868, HG03212, HG03045, HG02420, NA19036, HG03225, HG02819, HG03054, HG03132, HG03511, HG02334, NA19175, HG03547, NA19184, HG03457, HG03563, HG03136, HG02817, NA18856, NA19113, HG03451, HG02332, NA19473, HG03473, HG02464, HG02317, HG03419, HG03025, NA19185, NA20786, HG03118, HG02343, HG02760

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3643752

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	47
Observed Complex	0
Frequency	n/a