A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115138



Internal ID21298404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:86634092..86636980hg38UCSC Ensembl
Innerchr15:87177323..87180211hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg382889
hg192889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097561, nssv14096224, nssv14096162, nssv14096120, nssv14096077
Samplessample222, sample146, sample96, sample176, sample127
Known GenesAGBL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115138
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer