A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994620



Internal ID21903963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98693092..98755849hg38UCSC Ensembl
chr3:98411936..98474693hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3862758
hg1962758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549362
Samples
Known GenesST3GAL6, ST3GAL6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994620
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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