A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099965



Internal ID21276164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14644284..14969430hg38UCSC Ensembl
Innerchr20:14624930..14950076hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38325147
hg19325147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116941
Supporting Variants
Samplessample232
Known GenesMACROD2, MACROD2-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099965
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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