A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4273n100



Internal ID20155889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14887707..15064766hg38UCSC Ensembl
chr20:14868353..15045412hg19UCSC Ensembl
chr20:14816353..14993412hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38177060
hg19177060
hg18177060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059656, nsv1061643
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)dgv4273n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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