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nsv5708643

  • 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: 178 SVs from 29 studies. See in: genome view    
Submitted genomic74,658,654-74,658,654Question Mark
Overlapping variant regions from other studies: 178 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):74,950,995-74,950,995Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5708643Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1574,658,65474,658,654
nsv5708643RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1574,950,99574,950,995

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17197861alu insertionSequencingOther
nssv17228071alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17197861Submitted genomicNC_000015.10:g.746
58654_74658655ins2
79
GRCh38 (hg38)NC_000015.10Chr1574,658,65474,658,654
nssv17228071Submitted genomicNC_000015.10:g.746
58654_74658655ins2
79
GRCh38 (hg38)NC_000015.10Chr1574,658,65474,658,654
nssv17197861RemappedPerfectNC_000015.9:g.7495
0995_74950996ins27
9
GRCh37.p13First PassNC_000015.9Chr1574,950,99574,950,995
nssv17228071RemappedPerfectNC_000015.9:g.7495
0995_74950996ins27
9
GRCh37.p13First PassNC_000015.9Chr1574,950,99574,950,995

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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