A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700862



Internal ID15437514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:79036372..79037030hg38UCSC Ensembl
Innerchr9:81651288..81651946hg19UCSC Ensembl
Innerchr9:80841108..80841766hg18UCSC Ensembl
Innerchr9:78880842..78881500hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38659
hg19659
hg18659
hg17659
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524858
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700862
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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