A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3740e59



Internal ID22764960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2878992..2880390hg38UCSC Ensembl
chr7:2918626..2920024hg19UCSC Ensembl
chr7:2885152..2886550hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3353717, esv3391477
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3740e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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