A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174827



Internal ID15872694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70230432..70247989hg38UCSC Ensembl
Innerchr11:70076538..70094095hg19UCSC Ensembl
Innerchr11:69754186..69771743hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3817558
hg1917558
hg1817558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555383
Supporting Variants
SamplesHGDP00017
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174827
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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