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nsv5728773

  • Variant Calls:1
  • 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 28 studies. See in: genome view    
Submitted genomic173,609,434-173,609,434Question Mark
Overlapping variant regions from other studies: 101 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):173,036,437-173,036,437Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5728773Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5173,609,434173,609,434
nsv5728773RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5173,036,437173,036,437

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17241816line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17241816Submitted genomicNC_000005.10:g.173
609434_173609435in
s224
GRCh38 (hg38)NC_000005.10Chr5173,609,434173,609,434
nssv17241816RemappedPerfectNC_000005.9:g.1730
36437_173036438ins
224
GRCh37.p13First PassNC_000005.9Chr5173,036,437173,036,437

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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