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nsv5480009

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:429

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 78 SVs from 23 studies. See in: genome view    
Submitted genomic50,532,891-50,533,319Question Mark
Overlapping variant regions from other studies: 78 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):50,600,589-50,601,017Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5480009Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr750,532,89150,533,319
nsv5480009RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr750,600,58950,601,017

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16995677deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16995677Submitted genomicNC_000007.14:g.505
32891_50533319del
GRCh38 (hg38)NC_000007.14Chr750,532,89150,533,319
nssv16995677RemappedPerfectNC_000007.13:g.506
00589_50601017del
GRCh37.p13First PassNC_000007.13Chr750,600,58950,601,017

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)
nssv16995677<0.00116404
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