A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4049e59



Internal ID22765269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:7572820..7574718hg38UCSC Ensembl
chr8:7430342..7432240hg19UCSC Ensembl
chr8:7417752..7419650hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3432792, esv3382916
SamplesNA12891, NA19238
Known GenesFAM90A7P
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4049e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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