A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587883



Internal ID16375292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45968237..45978497hg38UCSC Ensembl
Innerchr21:47388151..47398411hg19UCSC Ensembl
Innerchr21:46212579..46222839hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810261
hg1910261
hg1810261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7910n54
Supporting Variantsnssv949168
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587883
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