A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728286



Internal ID151952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28196659..28214493hg38UCSC Ensembl
chr22:28592647..28610481hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3817835
hg1917835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146373
Supporting Variants
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728286
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002342


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