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nsv5720830

  • 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: 101 SVs from 24 studies. See in: genome view    
Submitted genomic152,479,901-152,479,901Question Mark
Overlapping variant regions from other studies: 101 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):152,801,036-152,801,036Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5720830Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6152,479,901152,479,901
nsv5720830RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6152,801,036152,801,036

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17235767line1 insertionSequencingOther
nssv17242831line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17235767Submitted genomicNC_000006.12:g.152
479901_152479902in
s1131
GRCh38 (hg38)NC_000006.12Chr6152,479,901152,479,901
nssv17242831Submitted genomicNC_000006.12:g.152
479901_152479902in
s1131
GRCh38 (hg38)NC_000006.12Chr6152,479,901152,479,901
nssv17235767RemappedPerfectNC_000006.11:g.152
801036_152801037in
s1131
GRCh37.p13First PassNC_000006.11Chr6152,801,036152,801,036
nssv17242831RemappedPerfectNC_000006.11:g.152
801036_152801037in
s1131
GRCh37.p13First PassNC_000006.11Chr6152,801,036152,801,036

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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