A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526809



Internal ID18478404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19032352hg38UCSC Ensembl
Innerchr14:19002112..19620039hg19UCSC Ensembl
Innerchr14:18072112..18690039hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38806718
hg19617928
hg18617928
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054177
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)nssv3526809
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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