A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528006



Internal ID18826287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18661498..19874569hg38UCSC Ensembl
Innerchr14:19437975..20342728hg19UCSC Ensembl
Innerchr14:18507975..19412568hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381213072
hg19904754
hg18904594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044073
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4M1, OR4N2, 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)nssv3528006
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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