A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539597



Internal ID314521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17885932..17886008hg38UCSC Ensembl
chr22:18368698..18368774hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727541
Samples
Known GenesMICAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539597
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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