A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4257n100



Internal ID20155873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14727124..15122658hg38UCSC Ensembl
chr20:14707770..15103304hg19UCSC Ensembl
chr20:14655770..15051304hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38395535
hg19395535
hg18395535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066377, nsv1062307, nsv1062274, nsv1059014
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)dgv4257n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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