A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4444n223



Internal ID22807412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33364820..33366447hg38UCSC Ensembl
chr20:31952626..31954253hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381628
hg191628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6596140, nsv6598161
Samples
Known GenesCDK5RAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4444n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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