A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097531



Internal ID21274407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97086146..97089386hg38UCSC Ensembl
Innerchr15:97629376..97632616hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg383241
hg193241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113396
Supporting Variants
Samplessample206
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097531
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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