A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451190



Internal ID229376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23320000..23325000hg38UCSC Ensembl
chr3:23361491..23366491hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385001
hg195001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930299
Samples
Known GenesUBE2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451190
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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