A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4264n100



Internal ID20155880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14775365..14952238hg38UCSC Ensembl
chr20:14756011..14932884hg19UCSC Ensembl
chr20:14704011..14880884hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38176874
hg19176874
hg18176874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056649, nsv1059009
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)dgv4264n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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