A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713382



Internal ID19011663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18497136..19956767hg38UCSC Ensembl
Innerchr14:19273613..20424926hg19UCSC Ensembl
Innerchr14:18343613..19494766hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381459632
hg191151314
hg181151154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037832
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)nssv3713382
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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