A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586481



Internal ID16027204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62143364..62158583hg38UCSC Ensembl
Innerchr20:60718420..60733639hg19UCSC Ensembl
Innerchr20:60151815..60167034hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3815220
hg1915220
hg1815220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942112
Samples
Known GenesPSMA7, SS18L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586481
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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