A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551054



Internal ID324541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49849108..49849535hg38UCSC Ensembl
chr22:50242756..50243183hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551054
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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