A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719627



Internal ID15666897
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 StatusS
Merged Variantsnsv546863
Supporting Variants
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)nssv719627
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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