A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374304



Internal ID21031857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33381710..33383941hg38UCSC Ensembl
chr3:33423202..33425433hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg382232
hg192232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210537
Samples
Known GenesFBXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374304
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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