A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656111



Internal ID21604416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63615130..63615130hg38UCSC Ensembl
chr11:63382602..63382602hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075619
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656111
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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