A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991313



Internal ID21900656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13291072..13297868hg38UCSC Ensembl
chr3:13332572..13339368hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386797
hg196797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991313
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