A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3120e59



Internal ID22764340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173399527..173399687hg38UCSC Ensembl
chr4:174320678..174320838hg19UCSC Ensembl
chr4:174557253..174557413hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38161
hg19161
hg18161
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302776, esv3302523
SamplesNA12717, NA11995, NA18508, NA10851, NA12414, NA11931, NA18603, NA18486, NA18545, NA12004, NA12750, NA07357, NA18940, NA12891, NA18558, NA18942, NA18582, NA18571, NA18949, NA12761, NA19238, NA19239, NA11993, NA11831, NA12878, NA18956, NA18948, NA18907, NA19114, NA11894, NA18912, NA12892, NA18853, NA19099, NA12144, NA18858, NA12043, NA18608, NA11881, NA19108, NA19240, NA18943, NA07037, NA12749, NA18609, NA19129, NA18577
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3120e59
Frequency
Sample Size185
Observed Gain47
Observed Loss0
Observed Complex0
Frequencyn/a


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