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nsv5549198

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,116

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 157 SVs from 37 studies. See in: genome view    
Submitted genomic41,574,318-41,606,433Question Mark
Overlapping variant regions from other studies: 157 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):41,970,322-42,002,437Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5549198Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2241,574,31841,606,433
nsv5549198RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2241,970,32242,002,437

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17729154duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17729154Submitted genomicNC_000022.11:g.415
74318_41606433dup
GRCh38 (hg38)NC_000022.11Chr2241,574,31841,606,433
nssv17729154RemappedPerfectNC_000022.10:g.419
70322_42002437dup
GRCh37.p13First PassNC_000022.10Chr2241,970,32242,002,437

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)
nssv17729154<0.00116404
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