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nsv5695062

  • 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: 292 SVs from 24 studies. See in: genome view    
Submitted genomic9,152,961-9,152,961Question Mark
Overlapping variant regions from other studies: 292 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):9,152,959-9,152,959Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5695062Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr189,152,9619,152,961
nsv5695062RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr189,152,9599,152,959

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17200781alu insertionSequencingOther
nssv17216210alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17200781Submitted genomicNC_000018.10:g.915
2961_9152962ins274		GRCh38 (hg38)NC_000018.10Chr189,152,9619,152,961
nssv17216210Submitted genomicNC_000018.10:g.915
2961_9152962ins274		GRCh38 (hg38)NC_000018.10Chr189,152,9619,152,961
nssv17200781RemappedPerfectNC_000018.9:g.9152
959_9152960ins274		GRCh37.p13First PassNC_000018.9Chr189,152,9599,152,959
nssv17216210RemappedPerfectNC_000018.9:g.9152
959_9152960ins274		GRCh37.p13First PassNC_000018.9Chr189,152,9599,152,959

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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