A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3447e59



Internal ID22764667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11490133..11492431hg38UCSC Ensembl
chr6:11490366..11492664hg19UCSC Ensembl
chr6:11598352..11600650hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg382299
hg192299
hg182299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3396914, esv3441435, esv3372842
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3447e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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