A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042228



Internal ID19131447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19424960..19954424hg38UCSC Ensembl
Innerchr14:20010901..20422583hg19UCSC Ensembl
Innerchr14:19080901..19492423hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38529465
hg19411683
hg18411523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1772n100
Supporting Variantsnssv3711181, nssv3527412, nssv3711180, nssv3527414, nssv3527413, nssv3711179, nssv3527411
Samples
Known GenesOR11H2, OR4K1, OR4K2, OR4K5, 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)nsv1042228
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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