A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515867



Internal ID292341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64116979..64132637hg38UCSC Ensembl
chr20:62748332..62763990hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3815659
hg1915659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515867
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer