A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705237



Internal ID21377513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117310195..117312214hg38UCSC Ensembl
chr11:117180911..117182930hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382020
hg192020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390041
Supporting Variants
Samples
Known GenesBACE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705237
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0172414


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