A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1659e59



Internal ID22762879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88379843..88381641hg38UCSC Ensembl
chr16:88446251..88448049hg19UCSC Ensembl
chr16:86973752..86975550hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3369724, esv3443468
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1659e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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