A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4221n100



Internal ID22790308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:449912..546851hg38UCSC Ensembl
chr20:430556..527495hg19UCSC Ensembl
chr20:378556..475495hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3896940
hg1996940
hg1896940
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055352, nsv1063600
Samples
Known GenesCSNK2A1, TBC1D20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4221n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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