A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202918



Internal ID20769958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4716031..4736362hg38UCSC Ensembl
chr20:4696677..4717008hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3820332
hg1920332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532395
Supporting Variants
Samples
Known GenesPRND, PRNT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202918
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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