A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115333



Internal ID21298599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:86634092..86638614hg38UCSC Ensembl
Innerchr15:87177323..87181845hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg384523
hg194523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv412n145
Supporting Variantsnssv14097096
Samplessample295
Known GenesAGBL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115333
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