A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051389



Internal ID19140608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18976182..19967215hg38UCSC Ensembl
Innerchr14:19562127..20435374hg19UCSC Ensembl
Innerchr14:18632127..19505214hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38991034
hg19873248
hg18873088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1766n100
Supporting Variantsnssv3529609, nssv3529610, nssv3529608
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)nsv1051389
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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