A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv374e59



Internal ID22761594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14447347..14450045hg38UCSC Ensembl
chr10:14489346..14492044hg19UCSC Ensembl
chr10:14529352..14532050hg18UCSC Ensembl
Cytoband10p13
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 Variantsesv3351774, esv3385890
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv374e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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