A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107296



Internal ID21283217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68475301..68552993hg38UCSC Ensembl
Innerchr4:69341019..69418711hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3877693
hg1977693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112439
Supporting Variants
Samplessample34
Known GenesTMPRSS11E, UGT2B17
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107296
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