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nsv5693415

  • 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: 91 SVs from 23 studies. See in: genome view    
Submitted genomic39,022,047-39,022,047Question Mark
Overlapping variant regions from other studies: 91 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):39,022,149-39,022,149Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5693415Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr539,022,04739,022,047
nsv5693415RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr539,022,14939,022,149

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17175416alu insertionSequencingOther
nssv17210929alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17175416Submitted genomicNC_000005.10:g.390
22047_39022048ins2
80		GRCh38 (hg38)NC_000005.10Chr539,022,04739,022,047
nssv17210929Submitted genomicNC_000005.10:g.390
22047_39022048ins2
80		GRCh38 (hg38)NC_000005.10Chr539,022,04739,022,047
nssv17175416RemappedPerfectNC_000005.9:g.3902
2149_39022150ins28
0		GRCh37.p13First PassNC_000005.9Chr539,022,14939,022,149
nssv17210929RemappedPerfectNC_000005.9:g.3902
2149_39022150ins28
0		GRCh37.p13First PassNC_000005.9Chr539,022,14939,022,149

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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