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nsv3565958

  • 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):Chaisson et al. 2019

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 447 SVs from 28 studies. See in: genome view    
Submitted genomic21,467,682-21,467,712Question Mark
Overlapping variant regions from other studies: 448 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):21,485,800-21,485,830Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3565958Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX21,467,697 (-15, +15)21,467,697 (-15, +15)
nsv3565958RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX21,485,815 (-15, +15)21,485,815 (-15, +15)

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
nssv14350013alu insertionSAMN00001694SequencingSequence alignmentHeterozygous16,419

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14350013Submitted genomicNC_000023.11:g.(21
467682_21467712)_(
21467682_21467712)
ins281
GRCh38 (hg38)NC_000023.11ChrX21,467,697 (-15, +15)21,467,697 (-15, +15)
nssv14350013RemappedPerfectNC_000023.10:g.(21
485800_21485830)_(
21485800_21485830)
ins281
GRCh37.p13First PassNC_000023.10ChrX21,485,815 (-15, +15)21,485,815 (-15, +15)

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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