A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586522



Internal ID16373931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62683890..62700093hg38UCSC Ensembl
Innerchr20:61315242..61331445hg19UCSC Ensembl
Innerchr20:60785687..60801890hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3816204
hg1916204
hg1816204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942277
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586522
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