A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3303142



Internal ID15150090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72420970..72420971hg38UCSC Ensembl
Innerchr11:72420901..72421040hg38UCSC Ensembl
Outerchr11:72420900..72421041hg38UCSC Ensembl
chr11:72132014..72132015hg19UCSC Ensembl
Innerchr11:72131945..72132084hg19UCSC Ensembl
Outerchr11:72131944..72132085hg19UCSC Ensembl
chr11:71809662..71809663hg18UCSC Ensembl
Innerchr11:71809732..71809593hg18UCSC Ensembl
Outerchr11:71809592..71809733hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38151
hg19151
hg18151
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7750078, essv7754689, essv7762486, essv7759158, essv7743843, essv7760378, essv7754201, essv7751512, essv7744376, essv7751140, essv7754394, essv7747485, essv7747136, essv7748434, essv7757708, essv7760450, essv7751647, essv7757517, essv7741194, essv7763160, essv7743543, essv7753905, essv7749006, essv7755432, essv7742950, essv7753684, essv7760739, essv7753826, essv7741764, essv7752700, essv7745792, essv7758086, essv7760640, essv7747799, essv7743125, essv7745993, essv7748795
SamplesNA18502, NA12717, NA11995, NA18861, NA18508, NA18980, NA18507, NA11931, NA19005, NA18944, NA12891, NA18942, NA18916, NA12287, NA12044, NA19239, NA12828, NA18973, NA11831, NA12489, NA12878, NA18956, NA18907, NA19114, NA11894, NA19225, NA18945, NA19108, NA18952, NA18517, NA19240, NA18943, NA12749, NA19116, NA18505, NA18511, NA18965
Known GenesCLPB
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3303142
Frequency
Sample Size185
Observed Gain37
Observed Loss0
Observed Complex0
Frequencyn/a


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