A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091182



Internal ID21291882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:129899843..129941492hg38UCSC Ensembl
Innerchr11:129769738..129811387hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3841650
hg1941650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115309
Supporting Variants
Samplessample80
Known GenesPRDM10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091182
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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