A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1645e59



Internal ID22762865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81614246..81615944hg38UCSC Ensembl
chr16:81647851..81649549hg19UCSC Ensembl
chr16:80205352..80207050hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3337516, esv3398010
SamplesNA19239, NA19240
Known GenesCMIP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1645e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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