A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660798



Internal ID21609103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47299623..47299623hg38UCSC Ensembl
chr11:47321174..47321174hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075036
SamplesHG00732
Known GenesMADD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660798
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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