A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4337e59



Internal ID22765557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65259074..65280788hg38UCSC Ensembl
chr9:42721656..42743354hg19UCSC Ensembl
chr9:42711652..42733350hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3821715
hg1921699
hg1821699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3434043, esv3394418
SamplesNA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4337e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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