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nsv5722964

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a L1 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: 232 SVs from 22 studies. See in: genome view    
Submitted genomic124,615,303-124,615,303Question Mark
Overlapping variant regions from other studies: 232 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):125,627,544-125,627,544Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5722964Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8124,615,303124,615,303
nsv5722964RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8125,627,544125,627,544

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17234771line1 insertionSequencingOther
nssv17236951line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17234771Submitted genomicNC_000008.11:g.124
615303_124615304in
s?
GRCh38 (hg38)NC_000008.11Chr8124,615,303124,615,303
nssv17236951Submitted genomicNC_000008.11:g.124
615303_124615304in
s?
GRCh38 (hg38)NC_000008.11Chr8124,615,303124,615,303
nssv17234771RemappedPerfectNC_000008.10:g.125
627544_125627545in
s?
GRCh37.p13First PassNC_000008.10Chr8125,627,544125,627,544
nssv17236951RemappedPerfectNC_000008.10:g.125
627544_125627545in
s?
GRCh37.p13First PassNC_000008.10Chr8125,627,544125,627,544

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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