A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3438e59



Internal ID22764658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:256452..383750hg38UCSC Ensembl
chr6:256452..383750hg19UCSC Ensembl
chr6:201452..328750hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38127299
hg19127299
hg18127299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3327033, esv3392251, esv3433883, esv3363744, esv3426938, esv3368743
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known GenesDUSP22
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3438e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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