A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587641



Internal ID16028364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42513540..42514449hg38UCSC Ensembl
Innerchr21:43933650..43934559hg19UCSC Ensembl
Innerchr21:42806719..42807628hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38910
hg19910
hg18910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7864n54
Supporting Variantsnssv947373, nssv947375, nssv947376, nssv947377, nssv947372, nssv947371, nssv947370, nssv947374
Samples
Known GenesSLC37A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587641
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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