A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044774



Internal ID18787305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19842764hg38UCSC Ensembl
Innerchr14:19002112..20310923hg19UCSC Ensembl
Innerchr14:18072112..19380763hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381617130
hg191308812
hg181308652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1753n100
Supporting Variantsnssv3526857, nssv3526856
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, OR11H2, 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)nsv1044774
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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