A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040757



Internal ID18783288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11874261..11955081hg38UCSC Ensembl
Innerchr11:11895808..11976628hg19UCSC Ensembl
Innerchr11:11852384..11933204hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3880821
hg1980821
hg1880821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3506154
Samples
Known GenesUSP47
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040757
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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