A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628928



Internal ID21820975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52909263..52914096hg38UCSC Ensembl
chr20:51525802..51530635hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384834
hg194834
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043778
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628928
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