A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054841



Internal ID18797372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89289516..89305785hg38UCSC Ensembl
Innerchr14:89755860..89772129hg19UCSC Ensembl
Innerchr14:88825613..88841882hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3816270
hg1916270
hg1816270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532578
Samples
Known GenesFOXN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054841
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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