A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3475e59



Internal ID20130224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32013297..32017395hg38UCSC Ensembl
chr6:31981074..31985172hg19UCSC Ensembl
chr6:32089052..32093150hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384099
hg194099
hg184099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3446536, esv3448152
SamplesNA19238, NA19239
Known GenesC4A, C4B, C4B_2, STK19
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3475e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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