A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776541



Internal ID15723811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55674892hg38UCSC Ensembl
Innerchr11:55373973..55442368hg19UCSC Ensembl
Innerchr11:55130549..55198944hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3868396
hg1968396
hg1868396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554921
Supporting Variants
Samples
Known GenesOR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv776541
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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