A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4375e59



Internal ID22765595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62445055..62455853hg38UCSC Ensembl
chr9:46756356..46767154hg19UCSC Ensembl
chr9:46596352..46607150hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3810799
hg1910799
hg1810799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3415048, esv3435683, esv3348222
SamplesNA12891, NA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4375e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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