A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv216e214



Internal ID22756110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87893226..87961083hg38UCSC Ensembl
chr11:87604118..87671975hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3867858
hg1967858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3627134, esv3627135
SamplesNA20877, NA20856
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv216e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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