A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053176



Internal ID18795707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19637241hg38UCSC Ensembl
Innerchr14:19002112..20105479hg19UCSC Ensembl
Innerchr14:18072112..19175240hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381411607
hg191103368
hg181103129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1752n100
Supporting Variantsnssv3526848, nssv3526849, nssv3713353, nssv3526847, nssv3526846, nssv3526845, nssv3713352
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, 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)nsv1053176
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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