A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100498



Internal ID22009731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53906088..53906088hg38UCSC Ensembl
chr19:54409342..54409342hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632031
Samples
Known GenesPRKCG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100498
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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