A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697447



Internal ID15434099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9860768..9872429hg38UCSC Ensembl
Innerchr8:9718278..9729939hg19UCSC Ensembl
Innerchr8:9755688..9767349hg18UCSC Ensembl
Innerchr8:9755688..9767349hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3811662
hg1911662
hg1811662
hg1711662
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520485
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697447
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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