A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1324e59



Internal ID22762544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94937462..94939460hg38UCSC Ensembl
chr14:95403799..95405797hg19UCSC Ensembl
chr14:94473552..94475550hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg381999
hg191999
hg181999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3374699, esv3417448
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1324e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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