A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154766



Internal ID22085271
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007259
Samples
Known GenesPGR
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154766
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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