A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113396



Internal ID21296662
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 StatusM
Merged Variantsdgv415n145
Supporting Variantsnssv14097531
Samplessample206
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113396
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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