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nsv5715973

  • Variant Calls:1
  • 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: 127 SVs from 20 studies. See in: genome view    
Submitted genomic232,100,507-232,100,507Question Mark
Overlapping variant regions from other studies: 127 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):232,965,217-232,965,217Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5715973Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2232,100,507232,100,507
nsv5715973RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2232,965,217232,965,217

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17252711sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17252711Submitted genomicNC_000002.12:g.232
100507_232100508in
s1240
GRCh38 (hg38)NC_000002.12Chr2232,100,507232,100,507
nssv17252711RemappedPerfectNC_000002.11:g.232
965217_232965218in
s1240
GRCh37.p13First PassNC_000002.11Chr2232,965,217232,965,217

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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