A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3332489



Internal ID15179476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133650036..133650036hg38UCSC Ensembl
Innerchr11:133650035..133650037hg38UCSC Ensembl
Outerchr11:133649976..133650086hg38UCSC Ensembl
chr11:133519931..133519931hg19UCSC Ensembl
Innerchr11:133519930..133519932hg19UCSC Ensembl
Outerchr11:133519871..133519981hg19UCSC Ensembl
chr11:133025141..133025141hg18UCSC Ensembl
Innerchr11:133025142..133025140hg18UCSC Ensembl
Outerchr11:133025081..133025191hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8811585
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3332489
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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