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nsv5550716

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:67

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 22 studies. See in: genome view    
Submitted genomic115,880,505-115,880,571Question Mark
Overlapping variant regions from other studies: 132 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):115,216,202-115,216,268Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5550716Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5115,880,505115,880,571
nsv5550716RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5115,216,202115,216,268

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16973721insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16973721Submitted genomicNC_000005.10:g.115
880505_115880571in
s59
GRCh38 (hg38)NC_000005.10Chr5115,880,505115,880,571
nssv16973721RemappedPerfectNC_000005.9:g.1152
16202_115216268ins
59
GRCh37.p13First PassNC_000005.9Chr5115,216,202115,216,268

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)
nssv16973721<0.00126404
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