A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710745



Internal ID18662340
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 StatusS
Merged Variantsnsv1038581
Supporting Variants
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)nssv3710745
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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