A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7885n223



Internal ID22810853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96637688..96640080hg38UCSC Ensembl
chr9:99399970..99402362hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382393
hg192393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6571145, nsv6560761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7885n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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