A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661375



Internal ID21609680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87438810..87438810hg38UCSC Ensembl
chr11:87149852..87149852hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075923
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661375
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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