A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687355



Internal ID111021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44579871..44579883hg38UCSC Ensembl
chr13:45154007..45154019hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422882
Supporting Variants
Samples
Known GenesTSC22D1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687355
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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