A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715497



Internal ID139163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66798238..66799584hg38UCSC Ensembl
chr17:64794356..64795702hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381347
hg191347
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425487
Supporting Variants
Samples
Known GenesPRKCA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715497
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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