A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652582



Internal ID21600887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118331227..118331227hg38UCSC Ensembl
chr11:118201942..118201942hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072757
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652582
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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