A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713332



Internal ID19011613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..18693031hg38UCSC Ensembl
Innerchr14:19002112..19469508hg19UCSC Ensembl
Innerchr14:18072112..18539508hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38467397
hg19467397
hg18467397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049013
Supporting Variants
Samples
Known GenesLOC642426, OR11H12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713332
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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