A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203819



Internal ID20770859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11787201..11860600hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3873400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549017
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203819
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.11224


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