A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097173



Internal ID21283644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68819497..68822890hg38UCSC Ensembl
Innerchr15:69111836..69115229hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383394
hg193394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117768
Supporting Variants
Samplessample348
Known GenesANP32A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097173
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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