A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534748



Internal ID310514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41566048..41566683hg38UCSC Ensembl
chr22:41962052..41962687hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729152
Samples
Known GenesCSDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534748
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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