A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661771



Internal ID21610076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134046061..134046061hg38UCSC Ensembl
chr11:133915956..133915956hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073321, nssv17073322
SamplesNA19650, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661771
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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