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nsv5731016

  • Variant Calls:2
  • 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: 124 SVs from 24 studies. See in: genome view    
Submitted genomic52,876,507-52,876,507Question Mark
Overlapping variant regions from other studies: 124 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):53,168,704-53,168,704Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5731016Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1552,876,50752,876,507
nsv5731016RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1553,168,70453,168,704

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17240664line1 insertionSequencingOther
nssv17240975line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17240664Submitted genomicNC_000015.10:g.528
76507_52876508ins2
354
GRCh38 (hg38)NC_000015.10Chr1552,876,50752,876,507
nssv17240975Submitted genomicNC_000015.10:g.528
76507_52876508ins2
354
GRCh38 (hg38)NC_000015.10Chr1552,876,50752,876,507
nssv17240664RemappedPerfectNC_000015.9:g.5316
8704_53168705ins23
54
GRCh37.p13First PassNC_000015.9Chr1553,168,70453,168,704
nssv17240975RemappedPerfectNC_000015.9:g.5316
8704_53168705ins23
54
GRCh37.p13First PassNC_000015.9Chr1553,168,70453,168,704

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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