A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116809



Internal ID21300075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61646904..61663478hg38UCSC Ensembl
Innerchr15:61939103..61955677hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3816575
hg1916575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097516
Samplessample197
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116809
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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