A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3446n223



Internal ID22806414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12849436..12850102hg38UCSC Ensembl
chr19:12960250..12960916hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6599441, nsv6596364
Samples
Known GenesMAST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3446n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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