A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591393



Internal ID16378802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:120443976..120446026hg38UCSC Ensembl
Innerchr3:120162823..120164873hg19UCSC Ensembl
Innerchr3:121645513..121647563hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382051
hg192051
hg182051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8523n54
Supporting Variantsnssv971758
Samples
Known GenesFSTL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591393
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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