A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046436



Internal ID19135655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19424960..19908283hg38UCSC Ensembl
Innerchr14:20010901..20376442hg19UCSC Ensembl
Innerchr14:19080901..19446282hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38483324
hg19365542
hg18365382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1772n100
Supporting Variantsnssv3527399, nssv3527401, nssv3527400
Samples
Known GenesOR11H2, OR4K2, OR4M1, OR4N2, OR4Q3, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046436
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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