A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116192



Internal ID21299458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112010372..112013991hg38UCSC Ensembl
Innerchr3:111729219..111732838hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg383620
hg193620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107802
Samplessample279
Known GenesTAGLN3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116192
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