A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704258



Internal ID127924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65269189..65269204hg38UCSC Ensembl
chr15:65561527..65561542hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543780
Supporting Variants
Samples
Known GenesPARP16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704258
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.017952


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