A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116316



Internal ID21299582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86505363..86511706hg38UCSC Ensembl
Innerchr16:86538969..86545312hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg386344
hg196344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097839
Samplessample373
Known GenesFENDRR, FOXF1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116316
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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