A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590094



Internal ID16030817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37941266..38021881hg38UCSC Ensembl
Innerchr3:37982757..38063372hg19UCSC Ensembl
Innerchr3:37957761..38038376hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3880616
hg1980616
hg1880616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962364
Samples
Known GenesCTDSPL, MIR26A1, PLCD1, VILL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590094
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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