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nsv5728972

  • 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: 212 SVs from 39 studies. See in: genome view    
Submitted genomic55,932,335-55,932,335Question Mark
Overlapping variant regions from other studies: 212 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):56,844,894-56,844,894Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5728972Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr855,932,33555,932,335
nsv5728972RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr856,844,89456,844,894

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17238621sva insertionSequencingOther
nssv17245593sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17238621Submitted genomicNC_000008.11:g.559
32335_55932336ins2
07
GRCh38 (hg38)NC_000008.11Chr855,932,33555,932,335
nssv17245593Submitted genomicNC_000008.11:g.559
32335_55932336ins2
07
GRCh38 (hg38)NC_000008.11Chr855,932,33555,932,335
nssv17238621RemappedPerfectNC_000008.10:g.568
44894_56844895ins2
07
GRCh37.p13First PassNC_000008.10Chr856,844,89456,844,894
nssv17245593RemappedPerfectNC_000008.10:g.568
44894_56844895ins2
07
GRCh37.p13First PassNC_000008.10Chr856,844,89456,844,894

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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