A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049115



Internal ID19138334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18976182..19908283hg38UCSC Ensembl
Innerchr14:19562127..20376442hg19UCSC Ensembl
Innerchr14:18632127..19446282hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38932102
hg19814316
hg18814156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1766n100
Supporting Variantsnssv3528206
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K2, 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)nsv1049115
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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