A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039959



Internal ID19129178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18976182..19856743hg38UCSC Ensembl
Innerchr14:19562127..20324902hg19UCSC Ensembl
Innerchr14:18632127..19394742hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38880562
hg19762776
hg18762616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1766n100
Supporting Variantsnssv3528201
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)nsv1039959
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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