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nsv5496254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 31 studies. See in: genome view    
Submitted genomic51,400,739-51,400,793Question Mark
Overlapping variant regions from other studies: 100 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):51,794,523-51,794,577Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1251,400,73951,400,793
nsv5496254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1251,794,52351,794,577

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058588deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058588Submitted genomicNC_000012.12:g.514
00739_51400793del
GRCh38 (hg38)NC_000012.12Chr1251,400,73951,400,793
nssv17058588RemappedPerfectNC_000012.11:g.517
94523_51794577del
GRCh37.p13First PassNC_000012.11Chr1251,794,52351,794,577

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)
nssv17058588<0.00116404
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