A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116983



Internal ID21300249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64990422..64990946hg38UCSC Ensembl
Innerchr15:65282760..65283284hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096161, nssv14097172
Samplessample146, sample348
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116983
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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