A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv766333



Internal ID16060289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6734551..6786012hg38UCSC Ensembl
Innerchr11:6755782..6807243hg19UCSC Ensembl
Innerchr11:6712358..6763819hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3851462
hg1951462
hg1851462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553376
Supporting Variants
Samples
Known GenesOR2AG1, OR2AG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv766333
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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