A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206816



Internal ID20773857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41187959..41193622hg38UCSC Ensembl
chr22:41583963..41589626hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg385664
hg195664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550385
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206816
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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