A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4283n100



Internal ID20155899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18364565..18647377hg38UCSC Ensembl
chr20:18345209..18628021hg19UCSC Ensembl
chr20:18293209..18576021hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38282813
hg19282813
hg18282813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065633, nsv1066436, nsv1067426
Samples
Known GenesDTD1, DZANK1, LINC00493, LINC00851, MIR3192, POLR3F, RBBP9, SEC23B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4283n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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