A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587560



Internal ID16374969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41687463..41713669hg38UCSC Ensembl
Innerchr21:43107623..43133829hg19UCSC Ensembl
Innerchr21:41980692..42006898hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3826207
hg1926207
hg1826207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7848n54
Supporting Variantsnssv947141
Samples
Known GenesLINC00111, LINC00479
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587560
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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