A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4285e59



Internal ID22765505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15984093..15984199hg38UCSC Ensembl
chr9:15984091..15984197hg19UCSC Ensembl
chr9:15974091..15974197hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38107
hg19107
hg18107
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302730, esv3302643
SamplesNA18502, NA18507, NA18870, NA18547, NA19138, NA19238, NA12878, NA18956, NA18907, NA19225, NA18570, NA19108, NA19240, NA19093, NA12776, NA18965
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4285e59
Frequency
Sample Size185
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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