nsv5678015

  • 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: 102 SVs from 26 studies. See in: genome view    
Submitted genomic39,336,848-39,336,848Question Mark
Overlapping variant regions from other studies: 102 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):39,336,950-39,336,950Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5678015Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr539,336,84839,336,848
nsv5678015RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr539,336,95039,336,950

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17175423alu insertionSequencingOther
nssv17210932alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17175423Submitted genomicNC_000005.10:g.393
36848_39336849ins2
71		GRCh38 (hg38)NC_000005.10Chr539,336,84839,336,848
nssv17210932Submitted genomicNC_000005.10:g.393
36848_39336849ins2
71		GRCh38 (hg38)NC_000005.10Chr539,336,84839,336,848
nssv17175423RemappedPerfectNC_000005.9:g.3933
6950_39336951ins27
1		GRCh37.p13First PassNC_000005.9Chr539,336,95039,336,950
nssv17210932RemappedPerfectNC_000005.9:g.3933
6950_39336951ins27
1		GRCh37.p13First PassNC_000005.9Chr539,336,95039,336,950

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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