A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691853



Internal ID115519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75901567..75975219hg38UCSC Ensembl
chr13:76475703..76549355hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3873653
hg1973653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502163
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691853
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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