A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007259



Internal ID22068890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:101032263..101056001hg38UCSC Ensembl
Outerchr11:101024724..101057558hg38UCSC Ensembl
Innerchr11:100902994..100926732hg19UCSC Ensembl
Outerchr11:100895455..100928289hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3832835
hg1932835
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154766
Supporting Variants
Samples
Known GenesPGR
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007259
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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