A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546863



Internal ID15987586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:97215786..97225449hg38UCSC Ensembl
Innerchr1:97681342..97691005hg19UCSC Ensembl
Innerchr1:97453930..97463593hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg389664
hg199664
hg189664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv719627, nssv719625, nssv719626, nssv719624
Samples
Known GenesDPYD, DPYD-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546863
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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