A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699760



Internal ID123426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42077745..42081959hg38UCSC Ensembl
chr15:42369943..42374157hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384215
hg194215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508878
Supporting Variants
Samples
Known GenesPLA2G4D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699760
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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