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nsv5707487

  • 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: 108 SVs from 26 studies. See in: genome view    
Submitted genomic76,539,075-76,539,075Question Mark
Overlapping variant regions from other studies: 108 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):76,932,855-76,932,855Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5707487Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1276,539,07576,539,075
nsv5707487RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1276,932,85576,932,855

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17232769alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17232769Submitted genomicNC_000012.12:g.765
39075_76539076ins2
79
GRCh38 (hg38)NC_000012.12Chr1276,539,07576,539,075
nssv17232769RemappedPerfectNC_000012.11:g.769
32855_76932856ins2
79
GRCh37.p13First PassNC_000012.11Chr1276,932,85576,932,855

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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