A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668764



Internal ID15405416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12400046..12439958hg38UCSC Ensembl
Innerchr7:12439672..12479584hg19UCSC Ensembl
Innerchr7:12406197..12446109hg18UCSC Ensembl
Innerchr7:12212912..12252824hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3839913
hg1939913
hg1839913
hg1739913
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516511
Supporting Variants
Samples
Known GenesVWDE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668764
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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