A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv775983



Internal ID15723253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55641224hg38UCSC Ensembl
Innerchr11:55371021..55408700hg19UCSC Ensembl
Innerchr11:55127597..55165276hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3837680
hg1937680
hg1837680
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554888
Supporting Variants
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv775983
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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