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nsv5685378

  • 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: 114 SVs from 27 studies. See in: genome view    
Submitted genomic36,224,698-36,224,698Question Mark
Overlapping variant regions from other studies: 114 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):36,226,320-36,226,320Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5685378Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr436,224,69836,224,698
nsv5685378RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr436,226,32036,226,320

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17208592alu insertionSequencingOther
nssv17230059alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17208592Submitted genomicNC_000004.12:g.362
24698_36224699ins2
81
GRCh38 (hg38)NC_000004.12Chr436,224,69836,224,698
nssv17230059Submitted genomicNC_000004.12:g.362
24698_36224699ins2
81
GRCh38 (hg38)NC_000004.12Chr436,224,69836,224,698
nssv17208592RemappedPerfectNC_000004.11:g.362
26320_36226321ins2
81
GRCh37.p13First PassNC_000004.11Chr436,226,32036,226,320
nssv17230059RemappedPerfectNC_000004.11:g.362
26320_36226321ins2
81
GRCh37.p13First PassNC_000004.11Chr436,226,32036,226,320

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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