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nsv5728511

  • 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: 135 SVs from 30 studies. See in: genome view    
Submitted genomic146,945,235-146,945,235Question Mark
Overlapping variant regions from other studies: 135 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):147,866,387-147,866,387Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5728511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4146,945,235146,945,235
nsv5728511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4147,866,387147,866,387

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17252572line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17252572Submitted genomicNC_000004.12:g.146
945235_146945236in
s241
GRCh38 (hg38)NC_000004.12Chr4146,945,235146,945,235
nssv17252572RemappedPerfectNC_000004.11:g.147
866387_147866388in
s241
GRCh37.p13First PassNC_000004.11Chr4147,866,387147,866,387

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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