A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930524



Internal ID21094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17066675..17067039hg38UCSC Ensembl
chr3:17108167..17108531hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446247
Supporting Variants
Samples
Known GenesPLCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930524
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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