A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586503



Internal ID16373912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62645662..62776055hg38UCSC Ensembl
Innerchr20:61277014..61407407hg19UCSC Ensembl
Innerchr20:60747459..60877852hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38130394
hg19130394
hg18130394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942126
Samples
Known GenesLINC00659, LOC100127888, NTSR1, SLCO4A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586503
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