A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585651



Internal ID16373060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16586557..16604669hg38UCSC Ensembl
Innerchr20:16567202..16585314hg19UCSC Ensembl
Innerchr20:16515202..16533314hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3818113
hg1918113
hg1818113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7507n54
Supporting Variantsnssv1152364, nssv1152361, nssv938578, nssv1152362, nssv1152363
SamplesHGDP00904, HGDP00934, HGDP00942, HGDP00921
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585651
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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