A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1790n223



Internal ID22804758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30432252..30433124hg38UCSC Ensembl
chr13:31006389..31007261hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6577758, nsv6583010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1790n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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