A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664963



Internal ID21613268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20338039..20338039hg38UCSC Ensembl
chr22:20325562..20325562hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg383960
hg193960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121552
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664963
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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