A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1665e59



Internal ID18987166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89428843..89430741hg38UCSC Ensembl
chr16:89495251..89497149hg19UCSC Ensembl
chr16:88022752..88024650hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3447688, esv3389864, esv3370088
SamplesNA19239, NA19238, NA19240
Known GenesANKRD11
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1665e59
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