A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4859n223



Internal ID22807827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46043135..46044091hg38UCSC Ensembl
chr3:46084627..46085583hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6552471, nsv6545108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4859n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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