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nsv5507622

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,516

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 158 SVs from 51 studies. See in: genome view    
Submitted genomic51,397,096-51,410,611Question Mark
Overlapping variant regions from other studies: 158 SVs from 51 studies. See in: genome view    
Remapped(Score: Perfect):51,790,880-51,804,395Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5507622Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1251,397,09651,410,611
nsv5507622RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1251,790,88051,804,395

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058587duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058587Submitted genomicNC_000012.12:g.513
97096_51410611dup
GRCh38 (hg38)NC_000012.12Chr1251,397,09651,410,611
nssv17058587RemappedPerfectNC_000012.11:g.517
90880_51804395dup
GRCh37.p13First PassNC_000012.11Chr1251,790,88051,804,395

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)
nssv17058587<0.00166404
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