A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990937



Internal ID21900280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105662955..105663028hg38UCSC Ensembl
chr3:105381799..105381872hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557386
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990937
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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