A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116252



Internal ID21483653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22619039..22619039hg38UCSC Ensembl
chr20:22599677..22599677hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670679
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116252
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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