A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591036



Internal ID16378445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96261349..96314798hg38UCSC Ensembl
Innerchr3:95980193..96033642hg19UCSC Ensembl
Innerchr3:97462883..97516332hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3853450
hg1953450
hg1853450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8452n54
Supporting Variantsnssv968100
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591036
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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