A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv118n97



Internal ID22815515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55756974..55808442hg38UCSC Ensembl
chr16:55790886..55842354hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3851469
hg1951469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155320, nsv1155323, nsv1155322, nsv1155321
Samples
Known GenesCES1, CES1P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv118n97
Frequency
Sample Size131
Observed Gain0
Observed Loss81
Observed Complex0
Frequencyn/a


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