A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3179e59



Internal ID22764399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100237..101935hg38UCSC Ensembl
chr5:100352..102050hg19UCSC Ensembl
chr5:153352..155050hg18UCSC Ensembl
Cytoband5p15.33
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 Variantsesv3335542, esv3329124
SamplesNA12891, NA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3179e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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