A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669107



Internal ID21617412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45032025..45032025hg38UCSC Ensembl
chr22:45427906..45427906hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130989
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669107
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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