A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5552737



Internal ID326054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26633829..26633829hg38UCSC Ensembl
chr22:27029793..27029793hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728208
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5552737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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