A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516511



Internal ID15443804
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668764, nssv672796
Samples
Known GenesVWDE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516511
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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