A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4399e59



Internal ID22765619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63315060..63343958hg38UCSC Ensembl
chr9:67270032..67298930hg19UCSC Ensembl
chr9:66959852..66988750hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3828899
hg1928899
hg1828899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3376931, esv3329481, esv3410639
SamplesNA19239, NA12878, NA12892
Known GenesAQP7P1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4399e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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