A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587336



Internal ID16374745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:26477027..26493659hg38UCSC Ensembl
Innerchr21:27849346..27865978hg19UCSC Ensembl
Innerchr21:26771217..26787849hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3816633
hg1916633
hg1816633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946587
Samples
Known GenesCYYR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587336
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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