A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175751



Internal ID15877469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122690917..122741587hg38UCSC Ensembl
Innerchr11:122561625..122612295hg19UCSC Ensembl
Innerchr11:122066835..122117505hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3850671
hg1950671
hg1850671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556480
Supporting Variants
SamplesHGDP00995
Known GenesUBASH3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175751
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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