A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732550



Internal ID156216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44435113..44436277hg38UCSC Ensembl
chr20:43063753..43064917hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381165
hg191165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732550
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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