A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093080



Internal ID21280437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111764555..111768228hg38UCSC Ensembl
Innerchr11:111635279..111638952hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg383674
hg193674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117534
Supporting Variants
Samplessample299
Known GenesPPP2R1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093080
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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