A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039767



Internal ID19128986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19915639hg38UCSC Ensembl
Innerchr14:19790343..20383798hg19UCSC Ensembl
Innerchr14:18860343..19453638hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38684691
hg19593456
hg18593296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1768n100
Supporting Variantsnssv3530927
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K2, OR4M1, OR4N2, OR4Q3, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039767
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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