A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122686



Internal ID21480424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:198219782..198219782hg38UCSC Ensembl
chr3:197946653..197946653hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615091
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122686
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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