A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527279



Internal ID18825560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19870678hg38UCSC Ensembl
Innerchr14:19801743..20338837hg19UCSC Ensembl
Innerchr14:18871743..19408677hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38639730
hg19537095
hg18536935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036497
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4M1, OR4N2, OR4Q3, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527279
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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