A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916478



Internal ID22691697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101139959..101161071hg38UCSC Ensembl
chr11:101010690..101031802hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3821113
hg1921113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352619
Samples
Known GenesLOC101054525
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916478
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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