A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672796



Internal ID15409448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12400046..12437852hg38UCSC Ensembl
Innerchr7:12439672..12477478hg19UCSC Ensembl
Innerchr7:12406197..12444003hg18UCSC Ensembl
Innerchr7:12212912..12250718hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3837807
hg1937807
hg1837807
hg1737807
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)nssv672796
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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