A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202160



Internal ID20769200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11509401..11516600hg38UCSC Ensembl
chr20:11490049..11497248hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202160
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00038


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