A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1770e59



Internal ID22762990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46494470..46496468hg38UCSC Ensembl
chr17:44571836..44573834hg19UCSC Ensembl
chr17:41927152..41929150hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381999
hg191999
hg181999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3398163, esv3369097
SamplesNA12891, NA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1770e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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