A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018479



Internal ID18761012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45935900..46865275hg38UCSC Ensembl
Innerchr8:46847522..47776897hg19UCSC Ensembl
Innerchr8:46966687..47896062hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38929376
hg19929376
hg18929376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7202n100
Supporting Variantsnssv3687392
Samples
Known GenesLINC00293
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018479
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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