A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097126



Internal ID21281513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32216980..32503619hg38UCSC Ensembl
Innerchr15:32509181..32795820hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38286640
hg19286640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115281
Supporting Variants
Samplessample312
Known GenesGOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097126
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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