A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4481e59



Internal ID22765701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92803749..92805447hg38UCSC Ensembl
chr9:95566031..95567729hg19UCSC Ensembl
chr9:94605852..94607550hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3435839, esv3394460
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4481e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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