A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622588



Internal ID7009446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21862627..21872268hg38UCSC Ensembl
Innerchr10:21862777..21872118hg38UCSC Ensembl
Outerchr10:21862477..21872418hg38UCSC Ensembl
chr10:22151556..22161197hg19UCSC Ensembl
Innerchr10:22151706..22161047hg19UCSC Ensembl
Outerchr10:22151406..22161347hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg389642
hg199642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13715476, essv13715482, essv13715478, essv13715479, essv13715480, essv13715477, essv13715483, essv13715481
SamplesNA19443, NA19098, NA18870, NA19198, HG02549, HG03114, HG02511, HG03376
Known GenesDNAJC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622588
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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