A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2519n223



Internal ID22805487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44827890..45072693hg38UCSC Ensembl
chr15:45120088..45364891hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38244804
hg19244804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6589130, nsv6587937
Samples
Known GenesC15orf43, SORD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2519n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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