A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029563



Internal ID21938906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59966289..59991793hg38UCSC Ensembl
chr16:60000193..60025697hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3825505
hg1925505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029563
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