A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553274



Internal ID20926383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33361032..33361446hg38UCSC Ensembl
chr3:33402524..33402938hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262041
Samples
Known GenesFBXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553274
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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