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nsv5715323

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a L1 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: 158 SVs from 25 studies. See in: genome view    
Submitted genomic89,597,939-89,597,939Question Mark
Overlapping variant regions from other studies: 158 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):90,307,658-90,307,658Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5715323Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr689,597,93989,597,939
nsv5715323RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr690,307,65890,307,658

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17248223line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17248223Submitted genomicNC_000006.12:g.895
97939_89597940ins4
5
GRCh38 (hg38)NC_000006.12Chr689,597,93989,597,939
nssv17248223RemappedPerfectNC_000006.11:g.903
07658_90307659ins4
5
GRCh37.p13First PassNC_000006.11Chr690,307,65890,307,658

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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