A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553241



Internal ID16340650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5484804..6182455hg38UCSC Ensembl
Innerchr11:5506034..6203685hg19UCSC Ensembl
Innerchr11:5462610..6160261hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38697652
hg19697652
hg18697652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv765366
Samples
Known GenesOR51B5, OR52B2, OR52B6, OR52D1, OR52E4, OR52E6, OR52E8, OR52H1, OR52L1, OR52N1, OR52N2, OR52N4, OR52N5, OR56A1, OR56A3, OR56A4, OR56A5, OR56B1, OR56B4, TRIM22, TRIM34, TRIM5, TRIM6, TRIM6-TRIM34, UBQLN3, UBQLNL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553241
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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