A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776667



Internal ID15723937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55618626..55684658hg38UCSC Ensembl
Innerchr11:55386102..55452134hg19UCSC Ensembl
Innerchr11:55142678..55208710hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3866033
hg1966033
hg1866033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554961
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)nssv776667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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