A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115012



Internal ID21298278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:72916640..72941282hg38UCSC Ensembl
Innerchr14:73383348..73407990hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3824643
hg1924643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094037
Samplessample17
Known GenesDCAF4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115012
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer