A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520318



Internal ID21844677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20815324..20815324hg38UCSC Ensembl
chr1:21141817..21141817hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053733
Supporting Variants
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520318
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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