A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694049



Internal ID117715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96988437..96989750hg38UCSC Ensembl
chr13:97640691..97642004hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381314
hg191314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510069
Supporting Variants
Samples
Known GenesOXGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694049
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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