A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525498



Internal ID21849856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4037014..4059232hg38UCSC Ensembl
chr3:4078698..4100916hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3822219
hg1922219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993453
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525498
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