A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1982e59



Internal ID22763202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6131241..6133939hg38UCSC Ensembl
chr19:6131252..6133950hg19UCSC Ensembl
chr19:6082252..6084950hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3397901, esv3363182
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1982e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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