A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3491e59



Internal ID22764711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35791897..35799495hg38UCSC Ensembl
chr6:35759674..35767272hg19UCSC Ensembl
chr6:35867652..35875250hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg387599
hg197599
hg187599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3330928, esv3431418, esv3410069, esv3345359
SamplesNA12891, NA19238, NA19239, NA12878
Known GenesCLPS
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3491e59
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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