A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698760



Internal ID15435412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60329303..60361006hg38UCSC Ensembl
Innerchr8:61241862..61273565hg19UCSC Ensembl
Innerchr8:61404416..61436119hg18UCSC Ensembl
Innerchr8:61404416..61436119hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3831704
hg1931704
hg1831704
hg1731704
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523071
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698760
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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