A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3208e59



Internal ID22764428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3727738..3728236hg38UCSC Ensembl
chr5:3727852..3728350hg19UCSC Ensembl
chr5:3780852..3781350hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38499
hg19499
hg18499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3336278, esv3371944
SamplesNA19238, NA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3208e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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