A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1966e59



Internal ID22763186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:431152..434850hg38UCSC Ensembl
chr19:431152..434850hg19UCSC Ensembl
chr19:382152..385850hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383699
hg193699
hg183699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3417174, esv3388466
SamplesNA19239, NA19240
Known GenesSHC2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1966e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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