A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007316



Internal ID22068947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112268501..112272273hg38UCSC Ensembl
Outerchr11:112266674..112277057hg38UCSC Ensembl
Innerchr11:112139224..112142996hg19UCSC Ensembl
Outerchr11:112137397..112147780hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3810384
hg1910384
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154776
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007316
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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