A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526806



Internal ID18478401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19019295hg38UCSC Ensembl
Innerchr14:19002112..19606995hg19UCSC Ensembl
Innerchr14:18072112..18676995hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38793661
hg19604884
hg18604884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055077
Supporting Variants
Samples
Known GenesLOC642426, OR11H12, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3526806
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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