A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4327e59



Internal ID22765547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40262438..40269436hg38UCSC Ensembl
chr9:42407456..42414454hg19UCSC Ensembl
chr9:42397452..42404450hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386999
hg196999
hg186999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3342096, esv3411851
SamplesNA12878, NA12892
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4327e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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