A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3694e59



Internal ID22764914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160612430..160633828hg38UCSC Ensembl
chr6:161033462..161054860hg19UCSC Ensembl
chr6:160953452..160974850hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3821399
hg1921399
hg1821399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3336819, esv3400353, esv3330598
SamplesNA19238, NA19239, NA19240
Known GenesLPA
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3694e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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