A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1797e59



Internal ID18987298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67025874..67026972hg38UCSC Ensembl
chr17:65021990..65023088hg19UCSC Ensembl
chr17:62452452..62453550hg18UCSC Ensembl
Cytoband17q24.2
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 Variantsesv3333825, esv3332466
SamplesNA19238, NA19240
Known GenesCACNG4
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1797e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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