A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045786



Internal ID18788317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19959442hg38UCSC Ensembl
Innerchr14:19002112..20427601hg19UCSC Ensembl
Innerchr14:18072112..19497441hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381733808
hg191425490
hg181425330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1753n100
Supporting Variantsnssv3713371, nssv3526896
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, 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)nsv1045786
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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