A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3717e59



Internal ID22764937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168714290..168716186hg38UCSC Ensembl
chr6:169114527..169116325hg19UCSC Ensembl
chr6:168856452..168858250hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381897
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3447644, esv3440511
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3717e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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