A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3807e59



Internal ID22765027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55166365..55167963hg38UCSC Ensembl
chr7:55234058..55235656hg19UCSC Ensembl
chr7:55201552..55203150hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3373783, esv3352178
SamplesNA19239, NA19240
Known GenesEGFR
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3807e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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