A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585777



Internal ID16373186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26252831..26320138hg38UCSC Ensembl
Innerchr20:26233467..26300774hg19UCSC Ensembl
Innerchr20:26181467..26248774hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3867308
hg1967308
hg1867308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939005, nssv939004
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585777
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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