A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv276n97



Internal ID22815673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8459149..8593314hg38UCSC Ensembl
chr8:8316659..8450824hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38134166
hg19134166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156834, nsv1156833
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv276n97
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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