A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1912n54



Internal ID20135336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55600413..55641224hg38UCSC Ensembl
chr11:55367889..55408700hg19UCSC Ensembl
chr11:55124465..55165276hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3840812
hg1940812
hg1840812
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554826, nsv554888, nsv554913
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1912n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss9
Observed Complex0
Frequencyn/a


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