A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6092n223



Internal ID22809060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23424631..23427370hg38UCSC Ensembl
chr6:23424859..23427598hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382740
hg192740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6562881, nsv6556463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6092n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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