A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938053



Internal ID15885323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14629311..14956289hg38UCSC Ensembl
Innerchr20:14609957..14936935hg19UCSC Ensembl
Innerchr20:14557957..14884935hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38326979
hg19326979
hg18326979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585453
Supporting Variants
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938053
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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