A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2982e59



Internal ID22764202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:49567378..49658076hg38UCSC Ensembl
chr4:49569395..49660093hg19UCSC Ensembl
chr4:49264152..49354850hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3890699
hg1990699
hg1890699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3429084, esv3424061, esv3365277
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2982e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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