A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587654



Internal ID16028377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42631745..42665548hg38UCSC Ensembl
Innerchr21:44051855..44085658hg19UCSC Ensembl
Innerchr21:42924924..42958727hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3833804
hg1933804
hg1833804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv947400
Samples
Known GenesPDE9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587654
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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