A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1588n54



Internal ID22769483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4785642..4862166hg38UCSC Ensembl
chr11:4806872..4883396hg19UCSC Ensembl
chr11:4763448..4839972hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3876525
hg1976525
hg1876525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553180, nsv553177, nsv553187
Samples
Known GenesOR51F2, OR51S1, OR52R1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1588n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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