A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994531



Internal ID21903874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98724044..98724480hg38UCSC Ensembl
chr3:98442888..98443324hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548765
Samples
Known GenesST3GAL6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994531
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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