A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585452



Internal ID16026175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14589296..15005956hg38UCSC Ensembl
Innerchr20:14569942..14986602hg19UCSC Ensembl
Innerchr20:14517942..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 Variantsdgv7465n54
Supporting Variantsnssv938052
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)nsv585452
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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