A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4966n223



Internal ID22807934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104784509..104785637hg38UCSC Ensembl
chr3:104503353..104504481hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg381129
hg191129
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6546622, nsv6541215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4966n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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