A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587333



Internal ID16374742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:26216516..26321228hg38UCSC Ensembl
Innerchr21:27588835..27693547hg19UCSC Ensembl
Innerchr21:26510706..26615418hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38104713
hg19104713
hg18104713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946584
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587333
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