A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553160



Internal ID16340569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4382962..4568337hg38UCSC Ensembl
Innerchr11:4404192..4589567hg19UCSC Ensembl
Innerchr11:4360768..4546143hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38185376
hg19185376
hg18185376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1583n54
Supporting Variantsnssv764649
Samples
Known GenesOR52K1, OR52K2, OR52M1, TRIM21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553160
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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