A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174789



Internal ID15877030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55679951..55822820hg38UCSC Ensembl
Innerchr11:55447427..55590296hg19UCSC Ensembl
Innerchr11:55204003..55346872hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38142870
hg19142870
hg18142870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555060
Supporting Variants
SamplesHGDP00926
Known GenesOR5D13, OR5D14, OR5D18, OR5L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174789
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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