A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2918e59



Internal ID22764138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1513819..1515829hg38UCSC Ensembl
chr4:1515546..1517556hg19UCSC Ensembl
chr4:1484852..1486850hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg382011
hg192011
hg181999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3331050, esv3332878
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2918e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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