A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687939



Internal ID111605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:55042169..55042220hg38UCSC Ensembl
chr13:55616304..55616355hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687939
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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