A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554799



Internal ID15995522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55315958..55641224hg38UCSC Ensembl
Innerchr11:55083434..55408700hg19UCSC Ensembl
Innerchr11:54840010..55165276hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38325267
hg19325267
hg18325267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174643
Samples1780854337_A
Known GenesOR4A15, OR4A16, OR4C11, OR4C15, OR4C16, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554799
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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