A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097096



Internal ID21280268
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 StatusS
Merged Variantsnsv3115333
Supporting Variants
Samplessample295
Known GenesAGBL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097096
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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