A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007199



Internal ID22068830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70171328..70174860hg38UCSC Ensembl
Outerchr11:70170311..70178971hg38UCSC Ensembl
Innerchr11:70017434..70020966hg19UCSC Ensembl
Outerchr11:70016417..70025077hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg388661
hg198661
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154745
Supporting Variants
Samples
Known GenesANO1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007199
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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