A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547380



Internal ID20920581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33341608..33342294hg38UCSC Ensembl
chr3:33383100..33383786hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262039
Samples
Known GenesFBXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547380
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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