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nsv4501498

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 18 SVs from 3 studies. See in: genome view    
Remapped(Score: Perfect):50,747,749-50,747,749Question Mark
Overlapping variant regions from other studies: 17 SVs from 3 studies. See in: genome view    
Submitted genomic48,825,110-48,825,110Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4501498RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1750,747,74950,747,749
nsv4501498Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1748,825,11048,825,110

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16017463alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16017463RemappedPerfectNC_000017.11:g.507
47749_50747750ins2
81
GRCh38.p12First PassNC_000017.11Chr1750,747,74950,747,749
nssv16017463Submitted genomicNC_000017.10:g.488
25110_48825111ins2
81
GRCh37.p13NC_000017.10Chr1748,825,11048,825,110

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)
nssv160174634.6e-005121694
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