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nsv5499536

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 45 studies. See in: genome view    
Submitted genomic51,403,106-51,403,157Question Mark
Overlapping variant regions from other studies: 121 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):51,796,890-51,796,941Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5499536Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1251,403,10651,403,157
nsv5499536RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1251,796,89051,796,941

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058589deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058589Submitted genomicNC_000012.12:g.514
03106_51403157del
GRCh38 (hg38)NC_000012.12Chr1251,403,10651,403,157
nssv17058589RemappedPerfectNC_000012.11:g.517
96890_51796941del
GRCh37.p13First PassNC_000012.11Chr1251,796,89051,796,941

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)
nssv170585890.2314646370
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