A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535569



Internal ID311188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41666301..41666784hg38UCSC Ensembl
chr22:42062305..42062788hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535569
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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