A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539825



Internal ID314699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65269173..65269190hg38UCSC Ensembl
chr15:65561511..65561528hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704257
Samples
Known GenesPARP16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539825
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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