A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592441



Internal ID16379850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164244697..164298228hg38UCSC Ensembl
Innerchr3:163962485..164016016hg19UCSC Ensembl
Innerchr3:165445179..165498710hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3853532
hg1953532
hg1853532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8715n54
Supporting Variantsnssv981113
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592441
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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