A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585543



Internal ID16372952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14886776..14986860hg38UCSC Ensembl
Innerchr20:14867422..14967506hg19UCSC Ensembl
Innerchr20:14815422..14915506hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38100085
hg19100085
hg18100085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7481n54
Supporting Variantsnssv938172
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)nsv585543
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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