A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526100



Internal ID302242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33514254..33523205hg38UCSC Ensembl
chr20:32102060..32111011hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg388952
hg198952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732027
Samples
Known GenesCBFA2T2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526100
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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