A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv227e214



Internal ID22756121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100410128..100522989hg38UCSC Ensembl
chr11:100280859..100393720hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38112862
hg19112862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3627484, esv3627481
SamplesHG01860, HG01801, HG01794, HG01805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv227e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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