A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587806



Internal ID16028529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44523374..44524882hg38UCSC Ensembl
Innerchr21:45943257..45944765hg19UCSC Ensembl
Innerchr21:44767685..44769193hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381509
hg191509
hg181509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7891n54
Supporting Variantsnssv948402
Samples
Known GenesTSPEAR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587806
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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