A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453622



Internal ID231738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101610448..101616411hg38UCSC Ensembl
chr3:101329292..101335255hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg385964
hg195964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453622
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