A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586909



Internal ID16374318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10560297..10754646hg38UCSC Ensembl
Innerchr21:10757811..10952160hg19UCSC Ensembl
Innerchr21:9779682..9974031hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38194350
hg19194350
hg18194350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7734n54
Supporting Variantsnssv944798
Samples
Known GenesTPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586909
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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