A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999726



Internal ID21909069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40643172..40662710hg38UCSC Ensembl
chr5:40643274..40662812hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3819539
hg1919539
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551338
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999726
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