A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4270n100



Internal ID20155886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14835657..15186129hg38UCSC Ensembl
chr20:14816303..15166775hg19UCSC Ensembl
chr20:14764303..15114775hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38350473
hg19350473
hg18350473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057120, nsv1059310
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)dgv4270n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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