A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713384



Internal ID19011665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18559262..19764467hg38UCSC Ensembl
Innerchr14:19335739..20232626hg19UCSC Ensembl
Innerchr14:18405739..19302466hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381205206
hg19896888
hg18896728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054019
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, OR11H2, OR4Q3, POTEG, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713384
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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