A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv899826



Internal ID6306837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:133155879..133212582hg19UCSC Ensembl
Outerchr12:133155424..133220526hg19UCSC Ensembl
Innerchr12:131665952..131722655hg18UCSC Ensembl
Outerchr12:131665497..131730599hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1549848
SamplesMS18276
Known GenesFBRSL1, LOC100507055, P2RX2, POLE
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv899826
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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