A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697490



Internal ID15434142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64029718..64142566hg38UCSC Ensembl
Innerchr10:65789478..65902327hg19UCSC Ensembl
Innerchr10:65459484..65572333hg18UCSC Ensembl
Innerchr10:65459484..65572333hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38112849
hg19112850
hg18112850
hg17112850
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520566
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697490
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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