A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727459



Internal ID151125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12607418..12607422hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38445
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727459
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.154207


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