A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174791



Internal ID15879713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55736145..55786621hg38UCSC Ensembl
Innerchr11:55503621..55554097hg19UCSC Ensembl
Innerchr11:55260197..55310673hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3850477
hg1950477
hg1850477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555076
Supporting Variants
SamplesHGDP01418
Known GenesOR5D13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174791
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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