A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv410e59



Internal ID22761630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46578473..46585171hg38UCSC Ensembl
chr10:46964446..46971144hg19UCSC Ensembl
chr10:46384452..46391150hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg386699
hg196699
hg186699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3383969, esv3385002
SamplesNA12878, NA12892
Known GenesSYT15
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv410e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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