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nsv5708294

  • 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: 122 SVs from 19 studies. See in: genome view    
Submitted genomic48,159,019-48,159,019Question Mark
Overlapping variant regions from other studies: 122 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):48,451,216-48,451,216Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5708294Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1548,159,01948,159,019
nsv5708294RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1548,451,21648,451,216

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17197765alu insertionSequencingOther
nssv17229295alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17197765Submitted genomicNC_000015.10:g.481
59019_48159020ins2
81
GRCh38 (hg38)NC_000015.10Chr1548,159,01948,159,019
nssv17229295Submitted genomicNC_000015.10:g.481
59019_48159020ins2
81
GRCh38 (hg38)NC_000015.10Chr1548,159,01948,159,019
nssv17197765RemappedPerfectNC_000015.9:g.4845
1216_48451217ins28
1
GRCh37.p13First PassNC_000015.9Chr1548,451,21648,451,216
nssv17229295RemappedPerfectNC_000015.9:g.4845
1216_48451217ins28
1
GRCh37.p13First PassNC_000015.9Chr1548,451,21648,451,216

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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