A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7687n223



Internal ID22810655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32481609..32482853hg38UCSC Ensembl
chr9:32481607..32482851hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6562741, nsv6572487
Samples
Known GenesDDX58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7687n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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