A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv55n97



Internal ID22815452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:662511..691425hg38UCSC Ensembl
chr12:771677..800591hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3828915
hg1928915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154789, nsv1154790
Samples
Known GenesNINJ2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv55n97
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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