A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533998



Internal ID309858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43464750..43464807hg38UCSC Ensembl
chr22:43860630..43860687hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729327
Samples
Known GenesMPPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533998
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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