A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058258



Internal ID18800789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73760658..74189316hg38UCSC Ensembl
Innerchr18:71427893..71856551hg19UCSC Ensembl
Innerchr18:69578873..70007531hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38428659
hg19428659
hg18428659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3400n100
Supporting Variantsnssv3563003
Samples
Known GenesFBXO15, TIMM21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058258
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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