A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520050



Internal ID296391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55215918..55216399hg38UCSC Ensembl
chr19:55727286..55727767hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725651
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520050
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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