A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533578



Internal ID309466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33586676..33597548hg38UCSC Ensembl
chr20:32174482..32185354hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3810873
hg1910873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732033
Samples
Known GenesCBFA2T2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533578
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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