A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7465n54



Internal ID20140889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14589296..15005956hg38UCSC Ensembl
chr20:14569942..14986602hg19UCSC Ensembl
chr20:14517942..14934602hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38416661
hg19416661
hg18416661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585453, nsv585454, nsv585452
Samples
Known GenesMACROD2, MACROD2-AS1, MACROD2-IT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7465n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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