nsv5698279

  • 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: 114 SVs from 16 studies. See in: genome view    
Submitted genomic71,117,872-71,117,872Question Mark
Overlapping variant regions from other studies: 114 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):69,114,013-69,114,013Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5698279Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1771,117,87271,117,872
nsv5698279RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1769,114,01369,114,013

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17200683alu insertionSequencingOther
nssv17214269alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17200683Submitted genomicNC_000017.11:g.711
17872_71117873ins1
01
GRCh38 (hg38)NC_000017.11Chr1771,117,87271,117,872
nssv17214269Submitted genomicNC_000017.11:g.711
17872_71117873ins1
01
GRCh38 (hg38)NC_000017.11Chr1771,117,87271,117,872
nssv17200683RemappedPerfectNC_000017.10:g.691
14013_69114014ins1
01
GRCh37.p13First PassNC_000017.10Chr1769,114,01369,114,013
nssv17214269RemappedPerfectNC_000017.10:g.691
14013_69114014ins1
01
GRCh37.p13First PassNC_000017.10Chr1769,114,01369,114,013

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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