A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446391



Internal ID224714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49546341..49546820hg38UCSC Ensembl
chr3:49583774..49584253hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446391
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