A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625516



Internal ID21817563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66304875..66304875hg38UCSC Ensembl
chr17:64300993..64300993hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082961
Supporting Variants
Samples
Known GenesPRKCA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625516
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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