A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3429e59



Internal ID20130178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176871545..176873543hg38UCSC Ensembl
chr5:176298546..176300544hg19UCSC Ensembl
chr5:176231152..176233150hg18UCSC Ensembl
Cytoband5q35.2
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 Variantsesv3381355, esv3401118
SamplesNA19239, NA19240
Known GenesUNC5A
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3429e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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