A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045598



Internal ID21954862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:361736..418964hg38UCSC Ensembl
chr20:342380..399608hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3857229
hg1957229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626468
Samples
Known GenesRBCK1, TRIB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045598
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