A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4491n223



Internal ID22807459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53633521..53633993hg38UCSC Ensembl
chr20:52250060..52250532hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6598171, nsv6598741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4491n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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