A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048171



Internal ID19137390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73499015..73560786hg38UCSC Ensembl
Innerchr11:73210060..73271831hg19UCSC Ensembl
Innerchr11:72887708..72949479hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3861772
hg1961772
hg1861772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510651
Samples
Known GenesFAM168A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048171
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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