A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5127n223



Internal ID22808095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189610393..189612590hg38UCSC Ensembl
chr3:189328182..189330379hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382198
hg192198
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6565159, nsv6558795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5127n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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