A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038759



Internal ID19127978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18605720..19964930hg38UCSC Ensembl
Innerchr14:19382197..20433089hg19UCSC Ensembl
Innerchr14:18452197..19502929hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381359211
hg191050893
hg181050733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1759n100
Supporting Variantsnssv3527027
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H2, OR4K1, OR4K2, OR4K5, 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)nsv1038759
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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