A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608222



Internal ID21800269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23853966..23853966hg38UCSC Ensembl
chr16:23865287..23865287hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094868
Supporting Variants
Samples
Known GenesPRKCB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608222
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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