A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5146n223



Internal ID22808114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7795440..7796943hg38UCSC Ensembl
chr4:7797167..7798670hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381504
hg191504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6570285, nsv6566108
Samples
Known GenesAFAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5146n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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