A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1627e59



Internal ID22762847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70155448..70163746hg38UCSC Ensembl
chr16:70189351..70197649hg19UCSC Ensembl
chr16:68746852..68755150hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg388299
hg198299
hg188299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3450061, esv3348253, esv3365753, esv3445572
SamplesNA19238, NA19239, NA12892, NA19240
Known GenesPDPR
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1627e59
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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