A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587381



Internal ID16028104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33321856..33323772hg38UCSC Ensembl
Innerchr21:34694161..34696077hg19UCSC Ensembl
Innerchr21:33616031..33617947hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381917
hg191917
hg181917
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7816n54
Supporting Variantsnssv946624, nssv946625
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587381
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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