A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516454



Internal ID292912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36024899..36025424hg38UCSC Ensembl
chr19:36515801..36516326hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723058
Samples
Known GenesCLIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516454
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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