A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4355e59



Internal ID22765575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42637765..42645363hg38UCSC Ensembl
chr9:44325756..44333354hg19UCSC Ensembl
chr9:44265752..44273350hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg387599
hg197599
hg187599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3397468, esv3335810, esv3326698
SamplesNA12891, NA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4355e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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