A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv59n206



Internal ID22755363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68850949..68865586hg38UCSC Ensembl
chr10:70610705..70625342hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3814638
hg1914638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5478085, nsv5476088
Samples
Known GenesSTOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv59n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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