A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890276



Internal ID22665303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18581979..18582095hg38UCSC Ensembl
chr3:18623471..18623587hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890276
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer