A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202923



Internal ID20769963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47372303..47376876hg38UCSC Ensembl
chr20:46001047..46005620hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg384574
hg194574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542457
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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