A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556479



Internal ID16343888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122687294..122741587hg38UCSC Ensembl
Innerchr11:122558002..122612295hg19UCSC Ensembl
Innerchr11:122063212..122117505hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3854294
hg1954294
hg1854294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2187n54
Supporting Variantsnssv1174961
SamplesHGDP01019
Known GenesUBASH3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556479
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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