A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1489n54



Internal ID22769384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133412162..133527325hg38UCSC Ensembl
chr10:135225666..135340829hg19UCSC Ensembl
chr10:135075656..135190819hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38115164
hg19115164
hg18115164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552685, nsv552652
Samples1780854418_A
Known GenesMTG1, SCART1, SPRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1489n54
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