A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1587n54



Internal ID22769482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4785476..4895859hg38UCSC Ensembl
chr11:4806706..4917089hg19UCSC Ensembl
chr11:4763282..4873665hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38110384
hg19110384
hg18110384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553179, nsv553182, nsv553184, nsv553185, nsv553188, nsv553181, nsv553183, nsv553176, nsv553178
Samples1780854058_A
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1587n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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