A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974479



Internal ID18263004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89460324..89472786hg38UCSC Ensembl
Innerchr14:89926668..89939130hg19UCSC Ensembl
Innerchr14:88996421..89008883hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3812463
hg1912463
hg1812463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761110
SamplesHGDP00521
Known GenesFOXN3
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974479
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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