A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546869



Internal ID15987592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:97787849..97862537hg38UCSC Ensembl
Innerchr1:98253405..98328093hg19UCSC Ensembl
Innerchr1:98025993..98100681hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3874689
hg1974689
hg1874689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv376n54
Supporting Variantsnssv719633
Samples
Known GenesDPYD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546869
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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