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nsv5501258

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:140

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 80 SVs from 19 studies. See in: genome view    
Submitted genomic51,505,104-51,505,243Question Mark
Overlapping variant regions from other studies: 80 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):51,898,888-51,899,027Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5501258Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1251,505,10451,505,243
nsv5501258RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1251,898,88851,899,027

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058596deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058596Submitted genomicNC_000012.12:g.515
05104_51505243del
GRCh38 (hg38)NC_000012.12Chr1251,505,10451,505,243
nssv17058596RemappedPerfectNC_000012.11:g.518
98888_51899027del
GRCh37.p13First PassNC_000012.11Chr1251,898,88851,899,027

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)
nssv17058596<0.00116404
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