A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096162



Internal ID21270022
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 StatusS
Merged Variantsnsv3115138
Supporting Variants
Samplessample146
Known GenesAGBL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096162
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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