A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091159



Internal ID21291294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111386710..111389916hg38UCSC Ensembl
Innerchr11:111257435..111260641hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg383207
hg193207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112489
Supporting Variants
Samplessample71
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091159
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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