A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696859



Internal ID15433511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:82346112..82369201hg38UCSC Ensembl
Innerchr8:83258347..83281436hg19UCSC Ensembl
Innerchr8:83420902..83443991hg18UCSC Ensembl
Innerchr8:83420902..83443991hg17UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3823090
hg1923090
hg1823090
hg1723090
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519448
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696859
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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