A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776585



Internal ID15723855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55607522..55676000hg38UCSC Ensembl
Innerchr11:55374998..55443476hg19UCSC Ensembl
Innerchr11:55131574..55200052hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3868479
hg1968479
hg1868479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554928
Supporting Variants
Samples
Known GenesOR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv776585
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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