A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649392



Internal ID21597697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22316770..22316770hg38UCSC Ensembl
chr11:22338316..22338316hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074121
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649392
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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