A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv302n97



Internal ID22815699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77151858..77171212hg38UCSC Ensembl
chr9:79766774..79786128hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3819355
hg1919355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154516, nsv1154513, nsv1154514
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv302n97
Frequency
Sample Size131
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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