A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699766



Internal ID123432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42128921..42141617hg38UCSC Ensembl
chr15:42421119..42433815hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3812697
hg1912697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494985
Supporting Variants
Samples
Known GenesPLA2G4F
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699766
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002811


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