A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039774



Internal ID18782305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89552535..89588132hg38UCSC Ensembl
Innerchr14:90018879..90054476hg19UCSC Ensembl
Innerchr14:89088632..89124229hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3835598
hg1935598
hg1835598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532579
Samples
Known GenesFOXN3, FOXN3-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039774
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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