A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655834



Internal ID21604139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116687997..116687997hg38UCSC Ensembl
chr11:116558713..116558713hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072830
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655834
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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