A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585537



Internal ID16026260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14859792..14889752hg38UCSC Ensembl
Innerchr20:14840438..14870398hg19UCSC Ensembl
Innerchr20:14788438..14818398hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3829961
hg1929961
hg1829961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7480n54
Supporting Variantsnssv1151232
SamplesHGDP00733
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585537
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer