A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2508n223



Internal ID22805476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43091143..43091651hg38UCSC Ensembl
chr15:43383341..43383849hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6577743, nsv6591363
Samples
Known GenesUBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2508n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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