A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv185n206



Internal ID22755489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101486791..101773813hg38UCSC Ensembl
chr15:102026996..102314016hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38287023
hg19287021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5530008, nsv5525830
Samples
Known GenesPCSK6, TARSL2, TM2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv185n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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