A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533795



Internal ID309674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4027867..4028031hg38UCSC Ensembl
chr20:4008514..4008678hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533795
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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