A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1908n54



Internal ID20135332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55592737..55722901hg38UCSC Ensembl
chr11:55360213..55490377hg19UCSC Ensembl
chr11:55116789..55246953hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38130165
hg19130165
hg18130165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554904, nsv554906, nsv554814
SamplesHGDP01296, HGDP01003
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1908n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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