A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902314



Internal ID6264241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104164522..104169017hg19UCSC Ensembl
Outerchr14:104163901..104170465hg19UCSC Ensembl
Innerchr14:103234275..103238770hg18UCSC Ensembl
Outerchr14:103233654..103240218hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1509355
SamplesSP54782
Known GenesKLC1, XRCC3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902314
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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