A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665388



Internal ID21613693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17330615..17330615hg38UCSC Ensembl
chr22:17811505..17811505hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122346
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665388
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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