A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7499n223



Internal ID22810467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132991387..132992265hg38UCSC Ensembl
chr8:134003632..134004510hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6570779, nsv6575282
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7499n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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