A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205254



Internal ID20772294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18890468..18915296hg38UCSC Ensembl
chr20:18871112..18895940hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3824829
hg1924829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521138
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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