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nsv5701239

  • 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: 216 SVs from 39 studies. See in: genome view    
Submitted genomic218,728-218,728Question Mark
Overlapping variant regions from other studies: 216 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):168,728-168,728Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5701239Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8218,728218,728
nsv5701239RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8168,728168,728

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17183298alu insertionSequencingOther
nssv17230406alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17183298Submitted genomicNC_000008.11:g.218
728_218729ins280
GRCh38 (hg38)NC_000008.11Chr8218,728218,728
nssv17230406Submitted genomicNC_000008.11:g.218
728_218729ins280
GRCh38 (hg38)NC_000008.11Chr8218,728218,728
nssv17183298RemappedPerfectNC_000008.10:g.168
728_168729ins280
GRCh37.p13First PassNC_000008.10Chr8168,728168,728
nssv17230406RemappedPerfectNC_000008.10:g.168
728_168729ins280
GRCh37.p13First PassNC_000008.10Chr8168,728168,728

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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