A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7926n223



Internal ID22810894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117837707..117838789hg38UCSC Ensembl
chr9:120599985..120601067hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6568667, nsv6560068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7926n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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