A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2623n223



Internal ID22805591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89885202..89886009hg38UCSC Ensembl
chr15:90428434..90429241hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6588997, nsv6580946
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2623n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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