A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585690



Internal ID21534238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123808260..123811090hg38UCSC Ensembl
chr11:123678968..123681798hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382831
hg192831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073067
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585690
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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