A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1759e59



Internal ID22762979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44589858..44591356hg38UCSC Ensembl
chr17:42667226..42668724hg19UCSC Ensembl
chr17:40022752..40024250hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3385839, esv3349191, esv3401873
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1759e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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