A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067252



Internal ID18809783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31895110..32003781hg38UCSC Ensembl
Innerchr18:29475073..29583744hg19UCSC Ensembl
Innerchr18:27729071..27837742hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38108672
hg19108672
hg18108672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564164
Samples
Known GenesTRAPPC8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067252
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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