A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17018719



Internal ID80121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133487920..133530374hg38UCSC Ensembl
chr8:134500163..134542617hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3842455
hg1942455
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559600
Supporting Variants
Samples
Known GenesST3GAL1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17018719
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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