A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv42n206



Internal ID22755346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17365142..17369591hg38UCSC Ensembl
chr10:17407141..17411590hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg384450
hg194450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5479200, nsv5488841
Samples
Known GenesST8SIA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv42n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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