A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204252



Internal ID20771292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10672801..10695100hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3822300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553522
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204252
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.27048


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