A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131793



Internal ID21463840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22441834..22441834hg38UCSC Ensembl
chr3:22483325..22483325hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616371
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131793
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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