A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083885



Internal ID21993118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23875582..23875582hg38UCSC Ensembl
chr16:23886903..23886903hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599125
Samples
Known GenesPRKCB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083885
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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