A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036376



Internal ID18778907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19119026hg38UCSC Ensembl
Innerchr14:19002112..19706746hg19UCSC Ensembl
Innerchr14:18072112..18776746hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38893392
hg19704635
hg18704635
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1750n100
Supporting Variantsnssv3713347, nssv3526818, nssv3713343, nssv3526816, nssv3526817, nssv3526829, nssv3526819, nssv3526821, nssv3713341, nssv3526828, nssv3713346, nssv3713340, nssv3713342, nssv3526823, nssv3526820, nssv3526827, nssv3526826, nssv3526825, nssv3713339, nssv3713345, nssv3526822, nssv3526830, nssv3713344, nssv3526824
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036376
Frequency
Sample Size29084
Observed Gain23
Observed Loss1
Observed Complex0
Frequencyn/a


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