A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2027e59



Internal ID20128776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55526473..55528671hg38UCSC Ensembl
chr19:56037840..56040038hg19UCSC Ensembl
chr19:60729652..60731850hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382199
hg192199
hg182199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3395916, esv3381723
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2027e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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