A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv160e214



Internal ID18980335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94735462..94815612hg38UCSC Ensembl
chr10:96495219..96575369hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3880151
hg1980151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3624257, esv3624259
SamplesHG00268
Known GenesCYP2C18, CYP2C19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv160e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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