A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115489



Internal ID21298755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102817160..102818165hg38UCSC Ensembl
Innerchr4:103738317..103739322hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381006
hg191006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092327
Samplessample254
Known GenesUBE2D3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115489
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