A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046960



Internal ID19136179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18976182..19831523hg38UCSC Ensembl
Innerchr14:19562127..20299682hg19UCSC Ensembl
Innerchr14:18632127..19369522hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38855342
hg19737556
hg18737396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1766n100
Supporting Variantsnssv3528200
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, 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)nsv1046960
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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