A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728298



Internal ID151964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28521105..28521131hg38UCSC Ensembl
chr22:28917093..28917119hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546941
Supporting Variants
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728298
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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