A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892389



Internal ID19183209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:72456544..72466225hg38UCSC Ensembl
Outerchr13:72456544..72466225hg38UCSC Ensembl
Innerchr13:73030682..73040363hg19UCSC Ensembl
Outerchr13:73030682..73040363hg19UCSC Ensembl
Innerchr13:71928683..71938364hg18UCSC Ensembl
Outerchr13:71928683..71938364hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg389682
hg199682
hg189682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798660
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892389
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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