A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1020n209



Internal ID22827095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20769287..20994800hg38UCSC Ensembl
chr19:20952093..21177606hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38225514
hg19225514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5977389, nsv5970427, nsv5977341
Samples
Known GenesZNF85
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1020n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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