A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730306



Internal ID153972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2224825..2385108hg38UCSC Ensembl
chr20:2205471..2365754hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38160284
hg19160284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522313
Supporting Variants
Samples
Known GenesTGM3, TGM6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730306
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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