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nsv5517414

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:243

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 76 SVs from 20 studies. See in: genome view    
Submitted genomic51,489,186-51,489,428Question Mark
Overlapping variant regions from other studies: 76 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):51,992,440-51,992,682Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5517414Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1951,489,18651,489,428
nsv5517414RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1951,992,44051,992,682

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724112deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724112Submitted genomicNC_000019.10:g.514
89186_51489428del
GRCh38 (hg38)NC_000019.10Chr1951,489,18651,489,428
nssv17724112RemappedPerfectNC_000019.9:g.5199
2440_51992682del
GRCh37.p13First PassNC_000019.9Chr1951,992,44051,992,682

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)
nssv17724112<0.00136404
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