A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4471e59



Internal ID22765691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88973117..88974815hg38UCSC Ensembl
chr9:91588032..91589730hg19UCSC Ensembl
chr9:90777852..90779550hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3375962, esv3399728, esv3381310
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4471e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer