A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205289



Internal ID20772329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51754417..51787009hg38UCSC Ensembl
chr20:50370956..50403548hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3832593
hg1932593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535747
Supporting Variants
Samples
Known GenesATP9A, SALL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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