A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047036



Internal ID15900222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180692918..180786878hg38UCSC Ensembl
Innerchr5:180119918..180213878hg19UCSC Ensembl
Innerchr5:180052524..180146484hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3893961
hg1993961
hg1893961
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600672
Supporting Variants
Samples
Known GenesOR2Y1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1047036
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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