A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553240



Internal ID16340649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5484804..5529400hg38UCSC Ensembl
Innerchr11:5506034..5550630hg19UCSC Ensembl
Innerchr11:5462610..5507206hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3844597
hg1944597
hg1844597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv765365
Samples
Known GenesOR51B5, OR52D1, UBQLN3, UBQLNL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553240
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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