A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4409e59



Internal ID22765629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40915718..41003301hg38UCSC Ensembl
chr9:68988947..69076530hg19UCSC Ensembl
chr9:68278752..68366350hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3887584
hg1987584
hg1887599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3332333, esv3418263, esv3411353, esv3382264, esv3335881, esv3349364
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4409e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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