A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520838



Internal ID297151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34800637..34805340hg38UCSC Ensembl
chr19:35291541..35296244hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384704
hg194704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520838
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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