A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3533059



Internal ID18484654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106625325..106877229hg38UCSC Ensembl
Innerchr14:107081339..107285437hg19UCSC Ensembl
Innerchr14:106152384..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38251905
hg19204099
hg18204099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045990
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3533059
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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