A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038581



Internal ID18781112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107693548..107967660hg38UCSC Ensembl
Innerchr11:107564274..107838386hg19UCSC Ensembl
Innerchr11:107069484..107343596hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38274113
hg19274113
hg18274113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1276n100
Supporting Variantsnssv3710745
Samples
Known GenesRAB39A, SLC35F2, SLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038581
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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