A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5543576



Internal ID317812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19248120..19249985hg38UCSC Ensembl
chr22:19235643..19237508hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381866
hg191866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727633
Samples
Known GenesCLTCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5543576
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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