A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054233



Internal ID19143452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19932624hg38UCSC Ensembl
Innerchr14:19790343..20400783hg19UCSC Ensembl
Innerchr14:18860343..19470623hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38701676
hg19610441
hg18610281
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1768n100
Supporting Variantsnssv3530929
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, 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)nsv1054233
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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