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nsv5717424

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a SVA 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: 159 SVs from 31 studies. See in: genome view    
Submitted genomic72,692,707-72,692,707Question Mark
Overlapping variant regions from other studies: 159 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):72,985,048-72,985,048Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5717424Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1572,692,70772,692,707
nsv5717424RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1572,985,04872,985,048

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17234824sva insertionSequencingOther
nssv17247732sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17234824Submitted genomicNC_000015.10:g.726
92707_72692708ins7
34
GRCh38 (hg38)NC_000015.10Chr1572,692,70772,692,707
nssv17247732Submitted genomicNC_000015.10:g.726
92707_72692708ins7
06
GRCh38 (hg38)NC_000015.10Chr1572,692,70772,692,707
nssv17234824RemappedPerfectNC_000015.9:g.7298
5048_72985049ins73
4
GRCh37.p13First PassNC_000015.9Chr1572,985,04872,985,048
nssv17247732RemappedPerfectNC_000015.9:g.7298
5048_72985049ins70
6
GRCh37.p13First PassNC_000015.9Chr1572,985,04872,985,048

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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