A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115168



Internal ID21298434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63499805..63508213hg38UCSC Ensembl
Innerchr15:63792004..63800412hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg388409
hg198409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096168
Samplessample149
Known GenesUSP3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115168
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