A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526866



Internal ID18478461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19926956hg38UCSC Ensembl
Innerchr14:19002112..20395115hg19UCSC Ensembl
Innerchr14:18072112..19464955hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381701322
hg191393004
hg181392844
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047691
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, OR11H2, 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)nssv3526866
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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