A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093189



Internal ID21283415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80159476..80162551hg38UCSC Ensembl
Innerchr11:79870520..79873595hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg383076
hg193076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115527
Supporting Variants
Samplessample344
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093189
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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