A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv242n97



Internal ID22815639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:316401..382559hg38UCSC Ensembl
chr6:316401..382559hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3866159
hg1966159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156442, nsv1156439, nsv1156445, nsv1156446, nsv1156440, nsv1156444, nsv1156443
Samples
Known GenesDUSP22
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv242n97
Frequency
Sample Size131
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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