A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1195n145



Internal ID22814211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102918937..102928125hg38UCSC Ensembl
chr8:103931165..103940353hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg389189
hg199189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117913, nsv3115903
Samplessample32, sample217, sample299, sample194
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1195n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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