A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519615



Internal ID295964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40813868..40813937hg38UCSC Ensembl
chr20:39442508..39442577hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519615
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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