A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1669e59



Internal ID22762889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90223343..90228341hg38UCSC Ensembl
chr16:90289751..90294749hg19UCSC Ensembl
chr16:88817252..88822250hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg384999
hg194999
hg184999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3336971, esv3404386, esv3435911, esv3421431
SamplesNA12891, NA19238, NA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1669e59
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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