A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1784n223



Internal ID22804752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27178793..27180040hg38UCSC Ensembl
chr13:27752930..27754177hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381248
hg191248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6579446, nsv6591703
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1784n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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