A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174299



Internal ID15878958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49289400..49416780hg38UCSC Ensembl
Innerchr11:49310952..49438332hg19UCSC Ensembl
Innerchr11:49267528..49394908hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38127381
hg19127381
hg18127381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554354
Supporting Variants
SamplesHGDP01285
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174299
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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