A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv178n206



Internal ID22755482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86980066..86986191hg38UCSC Ensembl
chr15:87523297..87529422hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg386126
hg196126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6144268, nsv5531363
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv178n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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