A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv14n206



Internal ID22755318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24017085..24023476hg38UCSC Ensembl
chr1:24343575..24349966hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386392
hg196392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5422197, nsv5427087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv14n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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