A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587709



Internal ID16028432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43739631..43743809hg38UCSC Ensembl
Innerchr21:45159512..45163690hg19UCSC Ensembl
Innerchr21:43983940..43988118hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg384179
hg194179
hg184179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7876n54
Supporting Variantsnssv948032
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587709
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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