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nsv5714135

  • 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: 154 SVs from 37 studies. See in: genome view    
Submitted genomic50,199,278-50,199,278Question Mark
Overlapping variant regions from other studies: 166 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):51,959,038-51,959,038Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5714135Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1050,199,27850,199,278
nsv5714135RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1051,959,03851,959,038

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17188527alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17188527Submitted genomicNC_000010.11:g.501
99278_50199279ins2
81
GRCh38 (hg38)NC_000010.11Chr1050,199,27850,199,278
nssv17188527RemappedPerfectNC_000010.10:g.519
59038_51959039ins2
81
GRCh37.p13First PassNC_000010.10Chr1051,959,03851,959,038

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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