A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695551



Internal ID119217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109576465..109576780hg38UCSC Ensembl
chr13:110228812..110229127hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494664
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695551
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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