A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587711



Internal ID16028434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43740010..43740206hg38UCSC Ensembl
Innerchr21:45159891..45160087hg19UCSC Ensembl
Innerchr21:43984319..43984515hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38197
hg19197
hg18197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948034
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587711
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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