A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689549



Internal ID15426201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50875899..50906089hg38UCSC Ensembl
Innerchr7:50943596..50973786hg19UCSC Ensembl
Innerchr7:50911090..50941280hg18UCSC Ensembl
Innerchr7:50717805..50747995hg17UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3830191
hg1930191
hg1830191
hg1730191
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520092
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689549
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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