A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527186



Internal ID303291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32862753..32877334hg38UCSC Ensembl
chr20:31450559..31465140hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3814582
hg1914582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527186
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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