A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589840



Internal ID16030563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16809700..16832586hg38UCSC Ensembl
Innerchr3:16851202..16874088hg19UCSC Ensembl
Innerchr3:16826206..16849092hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3822887
hg1922887
hg1822887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151742
SamplesHGDP00103
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589840
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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