A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3494n223



Internal ID22806462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31639147..31641430hg38UCSC Ensembl
chr19:32130053..32132336hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg382284
hg192284
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6596112, nsv6598623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3494n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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