A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038084



Internal ID19127303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18976182..19950786hg38UCSC Ensembl
Innerchr14:19562127..20418945hg19UCSC Ensembl
Innerchr14:18632127..19488785hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38974605
hg19856819
hg18856659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1766n100
Supporting Variantsnssv3528223
Samples
Known GenesBMS1P17, BMS1P18, 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)nsv1038084
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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