A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523062



Internal ID299311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23426820..23427652hg38UCSC Ensembl
chr19:23609622..23610454hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725048
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523062
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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