A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554440



Internal ID16341849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54541183..54930377hg38UCSC Ensembl
Innerchr11:51187354..51578097hg19UCSC Ensembl
Innerchr11:51043930..51434673hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38389195
hg19390744
hg18390744
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1823n54
Supporting Variantsnssv774045
Samples
Known GenesOR4A5, OR4C46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554440
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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