A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174608



Internal ID15879173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5878655..5933579hg38UCSC Ensembl
Innerchr11:5899885..5954809hg19UCSC Ensembl
Innerchr11:5856461..5911385hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3854925
hg1954925
hg1854925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553349
Supporting Variants
SamplesHGDP01321
Known GenesOR52E4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174608
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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