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nsv5730744

  • 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: 461 SVs from 25 studies. See in: genome view    
Submitted genomic29,441,630-29,441,630Question Mark
Overlapping variant regions from other studies: 462 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):29,459,747-29,459,747Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5730744Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX29,441,63029,441,630
nsv5730744RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX29,459,74729,459,747

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17202331alu insertionSequencingOther
nssv17228099alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17202331Submitted genomicNC_000023.11:g.294
41630_29441631ins2
80
GRCh38 (hg38)NC_000023.11ChrX29,441,63029,441,630
nssv17228099Submitted genomicNC_000023.11:g.294
41630_29441631ins2
80
GRCh38 (hg38)NC_000023.11ChrX29,441,63029,441,630
nssv17202331RemappedPerfectNC_000023.10:g.294
59747_29459748ins2
80
GRCh37.p13First PassNC_000023.10ChrX29,459,74729,459,747
nssv17228099RemappedPerfectNC_000023.10:g.294
59747_29459748ins2
80
GRCh37.p13First PassNC_000023.10ChrX29,459,74729,459,747

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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