A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096225



Internal ID21272353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97086254..97089374hg38UCSC Ensembl
Innerchr15:97629484..97632604hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg383121
hg193121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114073
Supporting Variants
Samplessample176
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096225
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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