A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1720e59



Internal ID22762940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:22741998..22763679hg38UCSC Ensembl
chr17:22241325..22263006hg19UCSC Ensembl
chr17:22165452..22187150hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg3821682
hg1921682
hg1821699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3416262, esv3427234, esv3442883, esv3370092, esv3373723
SamplesNA12891, NA19238, NA19239, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1720e59
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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