A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7889n223



Internal ID22810857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98041670..98042276hg38UCSC Ensembl
chr9:100803952..100804558hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6557982, nsv6562998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7889n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer