A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1402n54



Internal ID20134826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120457959..120469022hg38UCSC Ensembl
chr10:122217471..122228534hg19UCSC Ensembl
chr10:122207461..122218524hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3811064
hg1911064
hg1811064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552216, nsv552217
Samples
Known GenesPPAPDC1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1402n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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