A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203298



Internal ID20770338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34114358..34192321hg38UCSC Ensembl
chr20:32702164..32780127hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3877964
hg1977964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530216
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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