A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4613n223



Internal ID22807581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11373993..11377406hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6597748, nsv6599138, nsv6599917
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4613n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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