A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776843



Internal ID16070799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55692619..55836936hg38UCSC Ensembl
Innerchr11:55460095..55604412hg19UCSC Ensembl
Innerchr11:55216671..55360988hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38144318
hg19144318
hg18144318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555075
Supporting Variants
Samples
Known GenesOR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv776843
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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