A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv909584



Internal ID6271511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42214904..42300953hg19UCSC Ensembl
Outerchr18:42210808..42308972hg19UCSC Ensembl
Innerchr18:40468902..40554951hg18UCSC Ensembl
Outerchr18:40464806..40562970hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1564158
SamplesIS30171
Known GenesSETBP1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv909584
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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