A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694146



Internal ID117812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110088510..110111061hg38UCSC Ensembl
chr13:110740857..110763408hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3822552
hg1922552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694146
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001874


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