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nsv4566703

  • 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: 19 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):39,105,725-39,105,725Question Mark
Overlapping variant regions from other studies: 19 SVs from 5 studies. See in: genome view    
Submitted genomic39,147,216-39,147,216Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4566703RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr339,105,72539,105,725
nsv4566703Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr339,147,21639,147,216

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16045946sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16045946RemappedPerfectNC_000003.12:g.391
05725_39105726ins1
240
GRCh38.p12First PassNC_000003.12Chr339,105,72539,105,725
nssv16045946Submitted genomicNC_000003.11:g.391
47216_39147217ins1
240
GRCh37.p13NC_000003.11Chr339,147,21639,147,216

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)
nssv160459464.6e-005121694
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