A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044905



Internal ID19134124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18976182..19957752hg38UCSC Ensembl
Innerchr14:19562127..20425911hg19UCSC Ensembl
Innerchr14:18632127..19495751hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38981571
hg19863785
hg18863625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1766n100
Supporting Variantsnssv3529607, nssv3529606
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)nsv1044905
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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