A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352619



Internal ID22578288
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 StatusS
Merged Variantsnsv5916478
Supporting Variants
Samples
Known GenesLOC101054525
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352619
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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