A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1792n223



Internal ID22804760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31452370..31453872hg38UCSC Ensembl
chr13:32026507..32028009hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg381503
hg191503
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6578581, nsv6579360, nsv6586323
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1792n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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