A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553379



Internal ID15994102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6762170..6868698hg38UCSC Ensembl
Innerchr11:6783401..6889929hg19UCSC Ensembl
Innerchr11:6739977..6846505hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38106529
hg19106529
hg18106529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1626n54
Supporting Variantsnssv766335
Samples
Known GenesOR10A5, OR2AG1, OR2AG2, OR6A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553379
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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