A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036866



Internal ID19126085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18497136..19824020hg38UCSC Ensembl
Innerchr14:19273613..20292179hg19UCSC Ensembl
Innerchr14:18343613..19362019hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381326885
hg191018567
hg181018407
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1757n100
Supporting Variantsnssv3526911
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, 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)nsv1036866
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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