A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585549



Internal ID16026272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14903655..14933932hg38UCSC Ensembl
Innerchr20:14884301..14914578hg19UCSC Ensembl
Innerchr20:14832301..14862578hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3830278
hg1930278
hg1830278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7484n54
Supporting Variantsnssv938177
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)nsv585549
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