A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7910n223



Internal ID22810878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110466586..110467926hg38UCSC Ensembl
chr9:113228866..113230206hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381341
hg191341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6566641, nsv6559557
Samples
Known GenesSVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7910n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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