Variant Details

Variant: esv3644374

Internal ID

6684442

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr19:41186250..41191792	hg38	UCSC Ensembl
Inner	chr19:41186254..41191789	hg38	UCSC Ensembl
Outer	chr19:41186247..41191796	hg38	UCSC Ensembl
	chr19:41692155..41697697	hg19	UCSC Ensembl
Inner	chr19:41692159..41697694	hg19	UCSC Ensembl
Outer	chr19:41692152..41697701	hg19	UCSC Ensembl

Cytoband

19q13.2

Allele length

Assembly	Allele length
hg38	5543
hg19	5543

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv16055723, essv16055706, essv16055681, essv16055729, essv16055743, essv16055698, essv16055710, essv16055700, essv16055688, essv16055692, essv16055730, essv16055739, essv16055695, essv16055718, essv16055709, essv16055684, essv16055685, essv16055732, essv16055678, essv16055746, essv16055674, essv16055742, essv16055704, essv16055735, essv16055675, essv16055727, essv16055717, essv16055721, essv16055715, essv16055713, essv16055724, essv16055693, essv16055716, essv16055682, essv16055748, essv16055676, essv16055703, essv16055689, essv16055736, essv16055696, essv16055702, essv16055750, essv16055725, essv16055722, essv16055687, essv16055699, essv16055708, essv16055690, essv16055720, essv16055749, essv16055694, essv16055679, essv16055712, essv16055734, essv16055683, essv16055745, essv16055691, essv16055738, essv16055731, essv16055733, essv16055714, essv16055726, essv16055737, essv16055680, essv16055701, essv16055719, essv16055677, essv16055707, essv16055697, essv16055705, essv16055711, essv16055744, essv16055747, essv16055741, essv16055740, essv16055728, essv16055686

Samples

NA19394, HG01985, HG02339, HG03366, HG02944, HG02481, HG03052, NA19204, HG03300, HG03130, HG02870, NA19107, HG03464, NA19379, HG02952, HG02325, HG03485, HG03370, NA19131, HG02301, NA19197, HG02922, HG03079, NA19038, HG02505, NA19404, HG03268, HG02642, NA19172, HG02471, NA20127, HG02882, HG03169, HG02716, HG02943, HG03511, NA19347, NA18933, HG02511, NA19391, NA19455, HG03457, HG02953, HG01989, NA18871, HG02976, HG00740, HG03311, NA19114, HG02577, NA19031, NA19318, HG03354, HG02586, HG03109, HG02675, HG02484, HG01148, HG02667, NA19019, HG02546, HG02308, HG02983, NA19331, NA19144, NA19334, HG02464, HG02558, HG03103, NA19468, NA19096, HG01914, HG03118, HG02643, NA19429, NA19346, HG03265

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3644374

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	77
Observed Complex	0
Frequency	n/a