A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546865



Internal ID16334274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:97373331..97409107hg38UCSC Ensembl
Innerchr1:97838887..97874663hg19UCSC Ensembl
Innerchr1:97611475..97647251hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3835777
hg1935777
hg1835777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv719629
Samples
Known GenesDPYD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546865
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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