A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731706



Internal ID155372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24759688..24813264hg38UCSC Ensembl
chr20:24740324..24793900hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3853577
hg1953577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731706
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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