A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587716



Internal ID16028439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43740206..43756740hg38UCSC Ensembl
Innerchr21:45160087..45176621hg19UCSC Ensembl
Innerchr21:43984515..44001049hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3816535
hg1916535
hg1816535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948043
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587716
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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