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nsv5678219

  • 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: 411 SVs from 35 studies. See in: genome view    
Submitted genomic1,440,735-1,440,735Question Mark
Overlapping variant regions from other studies: 411 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):1,440,850-1,440,850Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5678219Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr51,440,7351,440,735
nsv5678219RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr51,440,8501,440,850

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17176800alu insertionSequencingOther
nssv17210905alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17176800Submitted genomicNC_000005.10:g.144
0735_1440736ins281
GRCh38 (hg38)NC_000005.10Chr51,440,7351,440,735
nssv17210905Submitted genomicNC_000005.10:g.144
0735_1440736ins281
GRCh38 (hg38)NC_000005.10Chr51,440,7351,440,735
nssv17176800RemappedPerfectNC_000005.9:g.1440
850_1440851ins281
GRCh37.p13First PassNC_000005.9Chr51,440,8501,440,850
nssv17210905RemappedPerfectNC_000005.9:g.1440
850_1440851ins281
GRCh37.p13First PassNC_000005.9Chr51,440,8501,440,850

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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