A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587479



Internal ID16374888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38910632..38925612hg38UCSC Ensembl
Innerchr21:40282556..40297536hg19UCSC Ensembl
Innerchr21:39204426..39219406hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3814981
hg1914981
hg1814981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946775
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587479
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