A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536372



Internal ID311865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37933415..37948986hg38UCSC Ensembl
chr22:38329422..38344993hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3815572
hg1915572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728892
Samples
Known GenesC22orf23, MICALL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536372
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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