A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899399



Internal ID375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20830866..20830917hg38UCSC Ensembl
chr1:21157359..21157410hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562165
Supporting Variants
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899399
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001094


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