A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529933



Internal ID305933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20023055..20023632hg38UCSC Ensembl
chr20:20003699..20004276hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731443
Samples
Known GenesNAA20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529933
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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