A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764682



Internal ID16058638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4798677..4862166hg38UCSC Ensembl
Innerchr11:4819907..4883396hg19UCSC Ensembl
Innerchr11:4776483..4839972hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3863490
hg1963490
hg1863490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553187
Supporting Variants
Samples
Known GenesOR51F2, OR51S1, OR52R1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764682
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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