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nsv5690929

  • Variant Calls:1
  • 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: 99 SVs from 19 studies. See in: genome view    
Submitted genomic69,774,337-69,774,337Question Mark
Overlapping variant regions from other studies: 99 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):70,001,469-70,001,469Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5690929Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr269,774,33769,774,337
nsv5690929RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr270,001,46970,001,469

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17206630alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17206630Submitted genomicNC_000002.12:g.697
74337_69774338ins2
79
GRCh38 (hg38)NC_000002.12Chr269,774,33769,774,337
nssv17206630RemappedPerfectNC_000002.11:g.700
01469_70001470ins2
79
GRCh37.p13First PassNC_000002.11Chr270,001,46970,001,469

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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