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nsv5709277

  • 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: 126 SVs from 21 studies. See in: genome view    
Submitted genomic55,393,985-55,393,985Question Mark
Overlapping variant regions from other studies: 125 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):53,471,346-53,471,346Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5709277Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1755,393,98555,393,985
nsv5709277RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1753,471,34653,471,346

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17200306alu insertionSequencingOther
nssv17217901alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17200306Submitted genomicNC_000017.11:g.553
93985_55393986ins2
81
GRCh38 (hg38)NC_000017.11Chr1755,393,98555,393,985
nssv17217901Submitted genomicNC_000017.11:g.553
93985_55393986ins2
81
GRCh38 (hg38)NC_000017.11Chr1755,393,98555,393,985
nssv17200306RemappedPerfectNC_000017.10:g.534
71346_53471347ins2
81
GRCh37.p13First PassNC_000017.10Chr1753,471,34653,471,346
nssv17217901RemappedPerfectNC_000017.10:g.534
71346_53471347ins2
81
GRCh37.p13First PassNC_000017.10Chr1753,471,34653,471,346

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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