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nsv5707749

  • 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: 195 SVs from 27 studies. See in: genome view    
Submitted genomic94,772,089-94,772,089Question Mark
Overlapping variant regions from other studies: 195 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):95,784,317-95,784,317Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5707749Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr894,772,08994,772,089
nsv5707749RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr895,784,31795,784,317

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17185006alu insertionSequencingOther
nssv17227592alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17185006Submitted genomicNC_000008.11:g.947
72089_94772090ins2
80
GRCh38 (hg38)NC_000008.11Chr894,772,08994,772,089
nssv17227592Submitted genomicNC_000008.11:g.947
72089_94772090ins2
80
GRCh38 (hg38)NC_000008.11Chr894,772,08994,772,089
nssv17185006RemappedPerfectNC_000008.10:g.957
84317_95784318ins2
80
GRCh37.p13First PassNC_000008.10Chr895,784,31795,784,317
nssv17227592RemappedPerfectNC_000008.10:g.957
84317_95784318ins2
80
GRCh37.p13First PassNC_000008.10Chr895,784,31795,784,317

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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