A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083836



Internal ID15590336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:49409771..49791123hg38UCSC Ensembl
Innerchr7:49449367..49830719hg19UCSC Ensembl
Innerchr7:49419913..49801265hg18UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg38381353
hg19381353
hg18381353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606896
Supporting Variants
Samples
Known GenesVWC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1083836
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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