A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520436



Internal ID15447729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133614712..133632326hg38UCSC Ensembl
Innerchr8:134626955..134644569hg19UCSC Ensembl
Innerchr8:134696137..134713751hg18UCSC Ensembl
Innerchr8:134696137..134713751hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3817615
hg1917615
hg1817615
hg1717615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671634, nssv701865, nssv671382
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520436
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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