A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1809n223



Internal ID22804777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40693888..40694873hg38UCSC Ensembl
chr13:41268024..41269009hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6577029, nsv6588667
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1809n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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