A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203451



Internal ID20770491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64284301..64292600hg38UCSC Ensembl
chr20:62915654..62923953hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548488
Supporting Variants
Samples
Known GenesLINC00266-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203451
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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