A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174649



Internal ID15527613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55592737..55679951hg38UCSC Ensembl
Innerchr11:55360213..55447427hg19UCSC Ensembl
Innerchr11:55116789..55204003hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3887215
hg1987215
hg1887215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554811
Supporting Variants
SamplesHGDP00520
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174649
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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