A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122166



Internal ID21448381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:16109327..16109327hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3856
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667597
Supporting Variants
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122166
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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