A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1986e59



Internal ID20128735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7841666..7843964hg38UCSC Ensembl
chr19:7906552..7908850hg19UCSC Ensembl
chr19:7812552..7814850hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382299
hg192299
hg182299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3361943, esv3347563, esv3426279, esv3450448
SamplesNA12891, NA19238, NA19239, NA19240
Known GenesEVI5L
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1986e59
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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