A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098197



Internal ID21288884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:83809054..83872312hg38UCSC Ensembl
Innerchr15:84477806..84541064hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3863259
hg1963259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117464
Supporting Variants
Samplessample423
Known GenesADAMTSL3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098197
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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