A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046328



Internal ID19135547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18661498..19785621hg38UCSC Ensembl
Innerchr14:19437975..20253780hg19UCSC Ensembl
Innerchr14:18507975..19323620hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381124124
hg19815806
hg18815646
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1761n100
Supporting Variantsnssv3714190, nssv3527999
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4M1, 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)nsv1046328
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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