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nsv5551639

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 149 SVs from 29 studies. See in: genome view    
Submitted genomic21,809,733-21,809,737Question Mark
Overlapping variant regions from other studies: 149 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):21,962,667-21,962,671Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5551639Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1221,809,73321,809,737
nsv5551639RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1221,962,66721,962,671

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17054012insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17054012Submitted genomicNC_000012.12:g.218
09733_21809737ins1
11
GRCh38 (hg38)NC_000012.12Chr1221,809,73321,809,737
nssv17054012RemappedPerfectNC_000012.11:g.219
62667_21962671ins1
11
GRCh37.p13First PassNC_000012.11Chr1221,962,66721,962,671

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17054012<0.00116404
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