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nsv5516282

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 21 studies. See in: genome view    
Submitted genomic28,061,064-28,061,134Question Mark
Overlapping variant regions from other studies: 162 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):25,641,028-25,641,098Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5516282Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1828,061,06428,061,134
nsv5516282RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1825,641,02825,641,098

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17716872duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17716872Submitted genomicNC_000018.10:g.280
61064_28061134dup
GRCh38 (hg38)NC_000018.10Chr1828,061,06428,061,134
nssv17716872RemappedPerfectNC_000018.9:g.2564
1028_25641098dup
GRCh37.p13First PassNC_000018.9Chr1825,641,02825,641,098

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)
nssv17716872<0.00116404
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