A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605098



Internal ID21553403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73806505..73806505hg38UCSC Ensembl
chr3:73855656..73855656hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381928
hg191928
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127967
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605098
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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