A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9583n54



Internal ID22777478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11310662..11312561hg38UCSC Ensembl
chr5:11310774..11312673hg19UCSC Ensembl
chr5:11363774..11365673hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381900
hg191900
hg181900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597146, nsv597148, nsv597147
Samples
Known GenesCTNND2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9583n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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