A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658611



Internal ID21606916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92944470..92944470hg38UCSC Ensembl
chr11:92677636..92677636hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38997
hg19997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076423
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658611
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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