A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437079



Internal ID215678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33576742..33576823hg38UCSC Ensembl
chr2:33801809..33801890hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16910473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437079
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