A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125226



Internal ID21507898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38290472..38290472hg38UCSC Ensembl
chr22:38686478..38686478hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666336
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125226
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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