A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443728



Internal ID222119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41048350..41103598hg38UCSC Ensembl
chr3:41089841..41145089hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3855249
hg1955249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443728
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