A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553273



Internal ID15993996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5618643..5850601hg38UCSC Ensembl
Innerchr11:5639873..5871831hg19UCSC Ensembl
Innerchr11:5596449..5828407hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38231959
hg19231959
hg18231959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv765572
Samples
Known GenesOR52E6, OR52N1, OR52N2, OR52N4, OR52N5, OR56B1, TRIM22, TRIM34, TRIM5, TRIM6-TRIM34
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553273
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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