A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3665n223



Internal ID22806633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43830622..43831930hg38UCSC Ensembl
chr19:44334774..44336082hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg381309
hg191309
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6598582, nsv6595802
Samples
Known GenesZNF283
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3665n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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