A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587668



Internal ID16028391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43401987..43415628hg38UCSC Ensembl
Innerchr21:44821867..44835508hg19UCSC Ensembl
Innerchr21:43646295..43659936hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3813642
hg1913642
hg1813642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7868n54
Supporting Variantsnssv947411
Samples
Known GenesSIK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587668
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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