A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2609n223



Internal ID22805577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83216166..83218643hg38UCSC Ensembl
chr15:83884918..83887395hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg382478
hg192478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6585911, nsv6591444
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2609n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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