A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055077



Internal ID18797608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19019295hg38UCSC Ensembl
Innerchr14:19002112..19606995hg19UCSC Ensembl
Innerchr14:18072112..18676995hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38793661
hg19604884
hg18604884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1749n100
Supporting Variantsnssv3713335, nssv3526806
Samples
Known GenesLOC642426, 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)nsv1055077
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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