A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761110



Internal ID17412630
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv974479
Supporting Variants
SamplesHGDP00521
Known GenesFOXN3
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761110
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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