A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036591



Internal ID19125810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18497136..19637241hg38UCSC Ensembl
Innerchr14:19273613..20105479hg19UCSC Ensembl
Innerchr14:18343613..19175240hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381140106
hg19831867
hg18831628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1757n100
Supporting Variantsnssv3713374, nssv3713375
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)nsv1036591
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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