A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991329



Internal ID21900672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137863901..137879851hg38UCSC Ensembl
chr3:137582743..137598693hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3815951
hg1915951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991329
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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