A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591671



Internal ID16379080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129596988..129606354hg38UCSC Ensembl
Innerchr3:129315831..129325197hg19UCSC Ensembl
Innerchr3:130798521..130807887hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg389367
hg199367
hg189367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8579n54
Supporting Variantsnssv973177
Samples
Known GenesPLXND1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591671
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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