A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698266



Internal ID15434918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:67639503..67640822hg38UCSC Ensembl
Innerchr1:68105186..68106505hg19UCSC Ensembl
Innerchr1:67877774..67879093hg18UCSC Ensembl
Innerchr1:67817207..67818526hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381320
hg191320
hg181320
hg171320
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521648
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698266
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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