A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534596



Internal ID310372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31921096..31921178hg38UCSC Ensembl
chr22:32317082..32317164hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534596
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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