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nsv5518960

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:63

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 239 SVs from 33 studies. See in: genome view    
Submitted genomic81,231,121-81,231,183Question Mark
Overlapping variant regions from other studies: 237 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):79,204,921-79,204,983Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518960Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1781,231,12181,231,183
nsv5518960RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1779,204,92179,204,983

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17715561deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17715561Submitted genomicNC_000017.11:g.812
31121_81231183del
GRCh38 (hg38)NC_000017.11Chr1781,231,12181,231,183
nssv17715561RemappedPerfectNC_000017.10:g.792
04921_79204983del
GRCh37.p13First PassNC_000017.10Chr1779,204,92179,204,983

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)
nssv17715561<0.00126404
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