A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4528e59



Internal ID22765748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129339352..129341150hg38UCSC Ensembl
chr9:132101631..132103429hg19UCSC Ensembl
chr9:131141452..131143250hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3446514, esv3331751, esv3374031
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4528e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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