A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174619



Internal ID15876359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:36602637..36876823hg38UCSC Ensembl
Innerchr11:36624187..36898373hg19UCSC Ensembl
Innerchr11:36580763..36854949hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38274187
hg19274187
hg18274187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554005
Supporting Variants
SamplesHGDP00828
Known GenesC11orf74
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174619
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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