A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7520n54



Internal ID22775415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24431218..24441617hg38UCSC Ensembl
chr20:24411854..24422253hg19UCSC Ensembl
chr20:24359854..24370253hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3810400
hg1910400
hg1810400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585739, nsv585741, nsv585740
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7520n54
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