A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669547



Internal ID21617852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33132512..33132512hg38UCSC Ensembl
chr22:33528498..33528498hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123222
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669547
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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