A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688817



Internal ID15078783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43808532..43815067hg38UCSC Ensembl
Innerchr8:43663675..43670210hg19UCSC Ensembl
Innerchr8:43782832..43789367hg18UCSC Ensembl
Innerchr8:43782832..43789367hg17UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg386536
hg196536
hg186536
hg176536
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519841
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688817
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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