A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695418



Internal ID15432070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:67400583..67407433hg38UCSC Ensembl
Innerchr8:68312818..68319668hg19UCSC Ensembl
Innerchr8:68475372..68482222hg18UCSC Ensembl
Innerchr8:68475372..68482222hg17UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg386851
hg196851
hg186851
hg176851
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518005
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695418
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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