A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902237



Internal ID6264164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101240530..101313093hg19UCSC Ensembl
Outerchr14:101233246..101320034hg19UCSC Ensembl
Innerchr14:100310283..100382846hg18UCSC Ensembl
Outerchr14:100302999..100389787hg18UCSC 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 Variantsnssv1543651
SamplesMS16153
Known GenesMEG3, MIR2392, MIR770
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902237
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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