A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202593



Internal ID20769633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30576601..30601000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3824400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526860
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202593
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00107


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