A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005524



Internal ID22067155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:274325..372369hg38UCSC Ensembl
Outerchr11:270715..377795hg38UCSC Ensembl
Innerchr11:274325..372369hg19UCSC Ensembl
Outerchr11:270715..377795hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38107081
hg19107081
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154668
Supporting Variants
Samples
Known GenesATHL1, B4GALNT4, IFITM1, IFITM2, IFITM3, IFITM5, NLRP6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005524
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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