A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776584



Internal ID15723854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55607522..55660224hg38UCSC Ensembl
Innerchr11:55374998..55427700hg19UCSC Ensembl
Innerchr11:55131574..55184276hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3852703
hg1952703
hg1852703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554927
Supporting Variants
Samples
Known GenesOR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv776584
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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