A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1425e214



Internal ID20122848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140953443..140965524hg38UCSC Ensembl
chr8:141963542..141975623hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3812082
hg1912082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3619045, esv3619044
SamplesHG03069
Known GenesPTK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1425e214
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