A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2666e59



Internal ID20129415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16177141..16178639hg38UCSC Ensembl
chr3:16218648..16220146hg19UCSC Ensembl
chr3:16193652..16195150hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3415457, esv3324120
SamplesNA19238, NA19239
Known GenesGALNT15
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2666e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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