A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5388n223



Internal ID22808356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102602303..102603244hg38UCSC Ensembl
chr4:103523460..103524401hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6563609, nsv6556955
Samples
Known GenesNFKB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5388n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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