A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2387n223



Internal ID22805355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23162501..23226400hg38UCSC Ensembl
chr15:22646668..22709832hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3863900
hg1963165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6506469, nsv6496310
Samples
Known GenesGOLGA8DP, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2387n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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