A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094037



Internal ID21271882
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 StatusS
Merged Variantsnsv3115012
Supporting Variants
Samplessample17
Known GenesDCAF4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094037
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