A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520092



Internal ID15447385
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv660638, nssv689549
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520092
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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