A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3326n223



Internal ID22806294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22645078..22646364hg38UCSC Ensembl
chr18:20225041..20226327hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381287
hg191287
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6587572, nsv6593872, nsv6593351
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3326n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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