A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587383



Internal ID16028106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33321856..33323970hg38UCSC Ensembl
Innerchr21:34694161..34696275hg19UCSC Ensembl
Innerchr21:33616031..33618145hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382115
hg192115
hg182115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7818n54
Supporting Variantsnssv946627, nssv946629, nssv946628
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587383
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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