A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1331e59



Internal ID22762551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99332462..99333260hg38UCSC Ensembl
chr14:99798799..99799597hg19UCSC Ensembl
chr14:98868552..98869350hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38799
hg19799
hg18799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3395529, esv3387831
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1331e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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