A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv222e214



Internal ID22756116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94823401..94855542hg38UCSC Ensembl
chr11:94556567..94588707hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3832142
hg1932141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3627330, esv3627329
SamplesHG03479, HG03025
Known GenesAMOTL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv222e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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