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nsv5521366

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,653

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 28 studies. See in: genome view    
Submitted genomic51,840,547-51,847,199Question Mark
Overlapping variant regions from other studies: 132 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):50,457,086-50,463,738Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521366Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2051,840,54751,847,199
nsv5521366RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2050,457,08650,463,738

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732958deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732958Submitted genomicNC_000020.11:g.518
40547_51847199del
GRCh38 (hg38)NC_000020.11Chr2051,840,54751,847,199
nssv17732958RemappedPerfectNC_000020.10:g.504
57086_50463738del
GRCh37.p13First PassNC_000020.10Chr2050,457,08650,463,738

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)
nssv17732958<0.00116404
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