A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526869



Internal ID18478464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19954424hg38UCSC Ensembl
Innerchr14:19002112..20422583hg19UCSC Ensembl
Innerchr14:18072112..19492423hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381728790
hg191420472
hg181420312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048306
Supporting Variants
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)nssv3526869
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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