A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7865n223



Internal ID22810833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86051014..86393052hg38UCSC Ensembl
chr9:88665929..89007967hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38342039
hg19342039
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6564425, nsv6562752
Samples
Known GenesC9orf153, GOLM1, ISCA1, ZCCHC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7865n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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