A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1685e59



Internal ID20128434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9227010..9228108hg38UCSC Ensembl
chr17:9130327..9131425hg19UCSC Ensembl
chr17:9071052..9072150hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3373663, esv3406770
SamplesNA19239, NA19238
Known GenesNTN1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1685e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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