A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587156



Internal ID16374565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18752126..18844403hg38UCSC Ensembl
Innerchr21:20124444..20216721hg19UCSC Ensembl
Innerchr21:19046315..19138592hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3892278
hg1992278
hg1892278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946158
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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