A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1786n223



Internal ID22804754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27732902..27734112hg38UCSC Ensembl
chr13:28307039..28308249hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg381211
hg191211
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6585562, nsv6586523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1786n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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