A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512369



Internal ID15505108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:89360382..89364067hg38UCSC Ensembl
Outerchr14:89826726..89830411hg19UCSC Ensembl
Outerchr14:88896479..88900164hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg383686
hg193686
hg183686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624956
Samples1
Known GenesFOXN3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512369
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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