A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2606n223



Internal ID22805574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81113301..81120100hg38UCSC Ensembl
chr15:81405642..81412441hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6500860, nsv6505787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2606n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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