A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648828



Internal ID21597133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119253539..119253539hg38UCSC Ensembl
chr11:119124249..119124249hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072560
SamplesHG00731
Known GenesCBL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648828
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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