A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3714e59



Internal ID20130463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167337474..167338872hg38UCSC Ensembl
chr6:167750962..167752360hg19UCSC Ensembl
chr6:167670952..167672350hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3361184, esv3435295, esv3382388
SamplesNA19239, NA19238, NA19240
Known GenesTTLL2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3714e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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