A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4268n100



Internal ID20155884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14820459..14931732hg38UCSC Ensembl
chr20:14801105..14912378hg19UCSC Ensembl
chr20:14749105..14860378hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38111274
hg19111274
hg18111274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063138, nsv1059476, nsv1065954, nsv1060833, nsv1064023, nsv1058879, nsv1059092, nsv1061473
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4268n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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