A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058079



Internal ID18800610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73970612..74118372hg38UCSC Ensembl
Innerchr18:71637847..71785607hg19UCSC Ensembl
Innerchr18:69788827..69936587hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38147761
hg19147761
hg18147761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563004
Samples
Known GenesFBXO15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058079
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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