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nsv5723033

  • 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: 145 SVs from 31 studies. See in: genome view    
Submitted genomic35,829,541-35,829,541Question Mark
Overlapping variant regions from other studies: 145 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):34,417,463-34,417,463Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5723033Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2035,829,54135,829,541
nsv5723033RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2034,417,46334,417,463

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17243980sva insertionSequencingOther
nssv17245676sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17243980Submitted genomicNC_000020.11:g.358
29541_35829542ins1
213
GRCh38 (hg38)NC_000020.11Chr2035,829,54135,829,541
nssv17245676Submitted genomicNC_000020.11:g.358
29541_35829542ins1
213
GRCh38 (hg38)NC_000020.11Chr2035,829,54135,829,541
nssv17243980RemappedPerfectNC_000020.10:g.344
17463_34417464ins1
213
GRCh37.p13First PassNC_000020.10Chr2034,417,46334,417,463
nssv17245676RemappedPerfectNC_000020.10:g.344
17463_34417464ins1
213
GRCh37.p13First PassNC_000020.10Chr2034,417,46334,417,463

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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