A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546871



Internal ID15987594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:97787849..97871727hg38UCSC Ensembl
Innerchr1:98253405..98337283hg19UCSC Ensembl
Innerchr1:98025993..98109871hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3883879
hg1983879
hg1883879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv376n54
Supporting Variantsnssv719635
Samples
Known GenesDPYD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546871
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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