A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038764



Internal ID19127983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18976182..19944629hg38UCSC Ensembl
Innerchr14:19562127..20412788hg19UCSC Ensembl
Innerchr14:18632127..19482628hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38968448
hg19850662
hg18850502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1766n100
Supporting Variantsnssv3714284
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)nsv1038764
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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