A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv765343



Internal ID16059299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5004970..5193183hg38UCSC Ensembl
Innerchr11:5026200..5214413hg19UCSC Ensembl
Innerchr11:4982776..5170989hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38188214
hg19188214
hg18188214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553219
Supporting Variants
Samples
Known GenesOR52A1, OR52A5, OR52E2, OR52J3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv765343
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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