A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205266



Internal ID20772306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20267283..20322356hg38UCSC Ensembl
chr20:20247927..20303000hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3855074
hg1955074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524778
Supporting Variants
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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