A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442345



Internal ID220773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135759572..135766174hg38UCSC Ensembl
chr3:135478414..135485016hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg386603
hg196603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442345
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