A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658333



Internal ID21606638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103049791..103049791hg38UCSC Ensembl
chr11:102920520..102920520hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071980
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658333
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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