A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902241



Internal ID6264168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101329709..101389678hg19UCSC Ensembl
Outerchr14:101323546..101394941hg19UCSC Ensembl
Innerchr14:100399462..100459431hg18UCSC Ensembl
Outerchr14:100393299..100464694hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1530789
SamplesMS10311
Known GenesMEG3, MEG8, MIR127, MIR136, MIR337, MIR431, MIR432, MIR433, MIR493, MIR665, RTL1, SNORD112, SNORD113-1, SNORD113-2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902241
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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