A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv194e214



Internal ID22756088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42421606..42498476hg38UCSC Ensembl
chr11:42443156..42520026hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3876871
hg1976871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3626113, esv3626114
SamplesHG01031, HG02075, HG03598
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv194e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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