A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554427



Internal ID16341836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54539077..55021565hg38UCSC Ensembl
Innerchr11:51095992..51580203hg19UCSC Ensembl
Innerchr11:50952568..51436779hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38482489
hg19484212
hg18484212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1823n54
Supporting Variantsnssv774016
Samples
Known GenesOR4A5, OR4C46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554427
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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