A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546872



Internal ID16334281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:97818298..97882219hg38UCSC Ensembl
Innerchr1:98283854..98347775hg19UCSC Ensembl
Innerchr1:98056442..98120363hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3863922
hg1963922
hg1863922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv377n54
Supporting Variantsnssv1173067
SamplesNINDS_199
Known GenesDPYD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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