A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203226



Internal ID20770266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22671968..22693138hg38UCSC Ensembl
chr20:22652606..22673776hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3821171
hg1921171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203226
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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