A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv54n97



Internal ID22815451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124212943..124232096hg38UCSC Ensembl
chr11:124083650..124102798hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3819154
hg1919149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154779, nsv1154778
Samples
Known GenesOR8G2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv54n97
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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