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nsv5727358

  • 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: 127 SVs from 23 studies. See in: genome view    
Submitted genomic73,863,932-73,863,932Question Mark
Overlapping variant regions from other studies: 127 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):74,776,167-74,776,167Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5727358Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr873,863,93273,863,932
nsv5727358RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr874,776,16774,776,167

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17239451line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17239451Submitted genomicNC_000008.11:g.738
63932_73863933ins6
015
GRCh38 (hg38)NC_000008.11Chr873,863,93273,863,932
nssv17239451RemappedPerfectNC_000008.10:g.747
76167_74776168ins6
015
GRCh37.p13First PassNC_000008.10Chr874,776,16774,776,167

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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