A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714189



Internal ID19012470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18661498..19732946hg38UCSC Ensembl
Innerchr14:19437975..20201105hg19UCSC Ensembl
Innerchr14:18507975..19270945hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381071449
hg19763131
hg18762971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038873
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, 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)nssv3714189
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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