A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719630



Internal ID16013586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:97538352..97613437hg38UCSC Ensembl
Innerchr1:98003908..98078993hg19UCSC Ensembl
Innerchr1:97776496..97851581hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3875086
hg1975086
hg1875086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546866
Supporting Variants
Samples
Known GenesDPYD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv719630
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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