A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554932



Internal ID15995655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55607522..55685196hg38UCSC Ensembl
Innerchr11:55374998..55452672hg19UCSC Ensembl
Innerchr11:55131574..55209248hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3877675
hg1977675
hg1877675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv776592
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)nsv554932
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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