A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6022n223



Internal ID22808990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168180631..168181801hg38UCSC Ensembl
chr5:167607636..167608806hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381171
hg191171
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6561235, nsv6571933
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6022n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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