A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4329e59



Internal ID22765549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40319238..40344636hg38UCSC Ensembl
chr9:42464256..42489654hg19UCSC Ensembl
chr9:42454252..42479650hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3825399
hg1925399
hg1825399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3369841, esv3451906
SamplesNA12878, NA12892
Known GenesFAM95B1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4329e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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