A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094636



Internal ID21283392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68475301..68732457hg38UCSC Ensembl
Innerchr4:69341019..69598175hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38257157
hg19257157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110364
Supporting Variants
Samplessample343
Known GenesTMPRSS11E, UGT2B15, UGT2B17
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094636
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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