A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731679



Internal ID155345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24374009..24379677hg38UCSC Ensembl
chr20:24354645..24360313hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg385669
hg195669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528303
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731679
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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