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nsv5713547

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a Alu mobile element relative to the reference
  • Publication(s):Chuang et al. 2021

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 172 SVs from 34 studies. See in: genome view    
Submitted genomic73,690,978-73,690,978Question Mark
Overlapping variant regions from other studies: 172 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):73,983,319-73,983,319Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5713547Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1573,690,97873,690,978
nsv5713547RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1573,983,31973,983,319

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17197852alu insertionSequencingOther
nssv17225927alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17197852Submitted genomicNC_000015.10:g.736
90978_73690979ins2
80
GRCh38 (hg38)NC_000015.10Chr1573,690,97873,690,978
nssv17225927Submitted genomicNC_000015.10:g.736
90978_73690979ins2
80
GRCh38 (hg38)NC_000015.10Chr1573,690,97873,690,978
nssv17197852RemappedPerfectNC_000015.9:g.7398
3319_73983320ins28
0
GRCh37.p13First PassNC_000015.9Chr1573,983,31973,983,319
nssv17225927RemappedPerfectNC_000015.9:g.7398
3319_73983320ins28
0
GRCh37.p13First PassNC_000015.9Chr1573,983,31973,983,319

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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