A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527997



Internal ID18826278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18661498..19758610hg38UCSC Ensembl
Innerchr14:19437975..20226769hg19UCSC Ensembl
Innerchr14:18507975..19296609hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381097113
hg19788795
hg18788635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049629
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, 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)nssv3527997
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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