A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664682



Internal ID21612987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50166025..50166025hg38UCSC Ensembl
chr22:50604454..50604454hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132037
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664682
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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