A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097223



Internal ID21285612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:86634092..86638922hg38UCSC Ensembl
Innerchr15:87177323..87182153hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg384831
hg194831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118051
Supporting Variants
Samplessample378
Known GenesAGBL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097223
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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