A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698278



Internal ID15434930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:76731333..76748315hg38UCSC Ensembl
Innerchr1:77197018..77214000hg19UCSC Ensembl
Innerchr1:76969606..76986588hg18UCSC Ensembl
Innerchr1:76909039..76926021hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3816983
hg1916983
hg1816983
hg1716983
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521661
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698278
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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