A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205885



Internal ID20772925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53715179..53720113hg38UCSC Ensembl
chr20:52331718..52336652hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384935
hg194935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539698
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205885
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.02347


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer