A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111139



Internal ID21294405
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 StatusM
Merged Variants
Supporting Variantsnssv14093430
Samplessample289
Known GenesTSPAN5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111139
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