A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553277



Internal ID15994000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5701718..5988845hg38UCSC Ensembl
Innerchr11:5722948..6010075hg19UCSC Ensembl
Innerchr11:5679524..5966651hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38287128
hg19287128
hg18287128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv765576
Samples
Known GenesOR52E4, OR52E6, OR52E8, OR52L1, OR52N1, OR52N2, OR52N4, OR52N5, OR56A3, OR56A5, OR56B1, TRIM22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553277
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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