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nsv5706040

  • 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: 130 SVs from 29 studies. See in: genome view    
Submitted genomic36,044,439-36,044,439Question Mark
Overlapping variant regions from other studies: 130 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):36,535,341-36,535,341Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5706040Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,044,43936,044,439
nsv5706040RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,535,34136,535,341

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17203044alu insertionSequencingOther
nssv17232236alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17203044Submitted genomicNC_000019.10:g.360
44439_36044440ins2
42
GRCh38 (hg38)NC_000019.10Chr1936,044,43936,044,439
nssv17232236Submitted genomicNC_000019.10:g.360
44439_36044440ins2
43
GRCh38 (hg38)NC_000019.10Chr1936,044,43936,044,439
nssv17203044RemappedPerfectNC_000019.9:g.3653
5341_36535342ins24
2
GRCh37.p13First PassNC_000019.9Chr1936,535,34136,535,341
nssv17232236RemappedPerfectNC_000019.9:g.3653
5341_36535342ins24
3
GRCh37.p13First PassNC_000019.9Chr1936,535,34136,535,341

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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