A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554928



Internal ID15995651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55607522..55676000hg38UCSC Ensembl
Innerchr11:55374998..55443476hg19UCSC Ensembl
Innerchr11:55131574..55200052hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3868479
hg1968479
hg1868479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv776585
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)nsv554928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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