A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4338e59



Internal ID22765558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65259474..65274883hg38UCSC Ensembl
chr9:42727556..42742954hg19UCSC Ensembl
chr9:42717552..42732950hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3815410
hg1915399
hg1815399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3347257, esv3435700
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4338e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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