A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713386



Internal ID19011667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18559262..19954424hg38UCSC Ensembl
Innerchr14:19335739..20422583hg19UCSC Ensembl
Innerchr14:18405739..19492423hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381395163
hg191086845
hg181086685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045976
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)nssv3713386
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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