A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646640



Internal ID21594945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110444696..110444696hg38UCSC Ensembl
chr11:110315420..110315420hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072489
SamplesHG02011
Known GenesFDX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646640
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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