A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590559



Internal ID16377968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66866359..66889990hg38UCSC Ensembl
Innerchr3:66916783..66940414hg19UCSC Ensembl
Innerchr3:66999473..67023104hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3823632
hg1923632
hg1823632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8364n54
Supporting Variantsnssv1152486
SamplesHGDP01163
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590559
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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