A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7906n223



Internal ID22810874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107308189..107309969hg38UCSC Ensembl
chr9:110070470..110072250hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381781
hg191781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6565040, nsv6573610
Samples
Known GenesRAD23B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7906n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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