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nsv5684277

  • 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: 84 SVs from 17 studies. See in: genome view    
Submitted genomic8,063,985-8,063,985Question Mark
Overlapping variant regions from other studies: 84 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):8,204,115-8,204,115Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5684277Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr28,063,9858,063,985
nsv5684277RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr28,204,1158,204,115

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17196254alu insertionSequencingOther
nssv17205863alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17196254Submitted genomicNC_000002.12:g.806
3985_8063986ins280		GRCh38 (hg38)NC_000002.12Chr28,063,9858,063,985
nssv17205863Submitted genomicNC_000002.12:g.806
3985_8063986ins281		GRCh38 (hg38)NC_000002.12Chr28,063,9858,063,985
nssv17196254RemappedPerfectNC_000002.11:g.820
4115_8204116ins280		GRCh37.p13First PassNC_000002.11Chr28,204,1158,204,115
nssv17205863RemappedPerfectNC_000002.11:g.820
4115_8204116ins281		GRCh37.p13First PassNC_000002.11Chr28,204,1158,204,115

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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