A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv464e59



Internal ID22761684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79376690..79379288hg38UCSC Ensembl
chr10:81136446..81139044hg19UCSC Ensembl
chr10:80806452..80809050hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382599
hg192599
hg182599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3400844, esv3351209
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv464e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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