A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733322



Internal ID156988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58033854..58036021hg38UCSC Ensembl
chr20:56608910..56611077hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg382168
hg192168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529946
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733322
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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