A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356448



Internal ID21014001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98723320..98757956hg38UCSC Ensembl
chr3:98442164..98476800hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3834637
hg1934637
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211295
Samples
Known GenesST3GAL6, ST3GAL6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356448
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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