A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587809



Internal ID16028532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44523881..44525236hg38UCSC Ensembl
Innerchr21:45943764..45945119hg19UCSC Ensembl
Innerchr21:44768192..44769547hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381356
hg191356
hg181356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7892n54
Supporting Variantsnssv948405
Samples
Known GenesTSPEAR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587809
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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