A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv162n97



Internal ID22815559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54215136..54249482hg38UCSC Ensembl
chr19:54719005..54753340hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3834347
hg1934336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155617, nsv1155619
Samples
Known GenesLILRA6, LILRB3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv162n97
Frequency
Sample Size131
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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