A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585563



Internal ID21534111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117121058..117121771hg38UCSC Ensembl
chr11:116991774..116992487hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072850
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585563
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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