A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4086n223



Internal ID22807054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113787654..113789722hg38UCSC Ensembl
chr2:114545231..114547299hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg382069
hg192069
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6537840, nsv6545743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4086n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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