A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553344



Internal ID16340753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5775532..5788000hg38UCSC Ensembl
Innerchr11:5796762..5809230hg19UCSC Ensembl
Innerchr11:5753338..5765806hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3812469
hg1912469
hg1812469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv766300, nssv766299, nssv766296, nssv766298, nssv766297
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553344
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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