A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527087



Internal ID18825368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18639702..19945687hg38UCSC Ensembl
Innerchr14:19416179..20413846hg19UCSC Ensembl
Innerchr14:18486179..19483686hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381305986
hg19997668
hg18997508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035296
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, 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)nssv3527087
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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