A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3178e59



Internal ID22764398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10001..11850hg38UCSC Ensembl
chr5:10001..11850hg19UCSC Ensembl
chr5:62952..64850hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381850
hg191850
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3451978, esv3365168, esv3365172, esv3368977, esv3445602, esv3340777
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3178e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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