A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4428e59



Internal ID22765648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65738515..65762413hg38UCSC Ensembl
chr9:70403632..70427530hg19UCSC Ensembl
chr9:69643452..69667350hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3823899
hg1923899
hg1823899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3376182, esv3348316, esv3446526, esv3415878, esv3447209
SamplesNA12891, NA19239, NA12878, NA12892, NA19240
Known GenesFOXD4L2, FOXD4L4
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4428e59
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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