A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591366



Internal ID16378775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119632551..119634816hg38UCSC Ensembl
Innerchr3:119351398..119353663hg19UCSC Ensembl
Innerchr3:120834088..120836353hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382266
hg192266
hg182266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8519n54
Supporting Variantsnssv971667
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591366
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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