A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045492



Internal ID19134711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107678441..107752052hg38UCSC Ensembl
Innerchr11:107549167..107622778hg19UCSC Ensembl
Innerchr11:107054377..107127988hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3873612
hg1973612
hg1873612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1275n100
Supporting Variantsnssv3514166
Samples
Known GenesSLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045492
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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