A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587805



Internal ID16028528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44523160..44524746hg38UCSC Ensembl
Innerchr21:45943043..45944629hg19UCSC Ensembl
Innerchr21:44767471..44769057hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381587
hg191587
hg181587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7891n54
Supporting Variantsnssv948401
Samples
Known GenesTSPEAR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587805
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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