A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688733



Internal ID15425385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88521862..88595208hg38UCSC Ensembl
Innerchr8:89534091..89607437hg19UCSC Ensembl
Innerchr8:89603207..89676553hg18UCSC Ensembl
Innerchr8:89603207..89676553hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3873347
hg1973347
hg1873347
hg1773347
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520279
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688733
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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