A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093430



Internal ID21279751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:98657555..98660254hg38UCSC Ensembl
Innerchr4:99578706..99581405hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111139
Supporting Variants
Samplessample289
Known GenesTSPAN5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093430
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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