A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714190



Internal ID19012471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18661498..19785621hg38UCSC Ensembl
Innerchr14:19437975..20253780hg19UCSC Ensembl
Innerchr14:18507975..19323620hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381124124
hg19815806
hg18815646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046328
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4M1, 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)nssv3714190
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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