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nsv5696477

  • 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: 129 SVs from 29 studies. See in: genome view    
Submitted genomic72,347,210-72,347,210Question Mark
Overlapping variant regions from other studies: 129 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):72,639,551-72,639,551Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5696477Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1572,347,21072,347,210
nsv5696477RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1572,639,55172,639,551

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17197843alu insertionSequencingOther
nssv17217355alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17197843Submitted genomicNC_000015.10:g.723
47210_72347211ins2
79
GRCh38 (hg38)NC_000015.10Chr1572,347,21072,347,210
nssv17217355Submitted genomicNC_000015.10:g.723
47210_72347211ins2
79
GRCh38 (hg38)NC_000015.10Chr1572,347,21072,347,210
nssv17197843RemappedPerfectNC_000015.9:g.7263
9551_72639552ins27
9
GRCh37.p13First PassNC_000015.9Chr1572,639,55172,639,551
nssv17217355RemappedPerfectNC_000015.9:g.7263
9551_72639552ins27
9
GRCh37.p13First PassNC_000015.9Chr1572,639,55172,639,551

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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