A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526546



Internal ID302672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2848766..2899014hg38UCSC Ensembl
chr19:2848764..2899012hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3850249
hg1950249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720471
Samples
Known GenesZNF555, ZNF556
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526546
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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