A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3658e59



Internal ID22764878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131698019..131710617hg38UCSC Ensembl
chr6:132019159..132031757hg19UCSC Ensembl
chr6:132060852..132073450hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3812599
hg1912599
hg1812599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3452154, esv3373672
SamplesNA12891, NA19238
Known GenesCTAGE9, ENPP3, OR2A4
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3658e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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