A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687854



Internal ID111520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53044433..53059463hg38UCSC Ensembl
chr13:53618568..53633598hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3815031
hg1915031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498468
Supporting Variants
Samples
Known GenesOLFM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687854
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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