A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616329



Internal ID21564634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133560768..133560768hg38UCSC Ensembl
chr3:133279612..133279612hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120148
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616329
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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