A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11n97



Internal ID22815408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88794408..88842283hg38UCSC Ensembl
chr1:89260091..89307966hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3847876
hg1947876
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156085, nsv1156086
Samples
Known GenesPKN2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv11n97
Frequency
Sample Size131
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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