A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4267n100



Internal ID22790354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14816926..14897834hg38UCSC Ensembl
chr20:14797572..14878480hg19UCSC Ensembl
chr20:14745572..14826480hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3880909
hg1980909
hg1880909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063838, nsv1058602
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)dgv4267n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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