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nsv4262351

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:962

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 53 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):3,199,447-3,200,408Question Mark
Overlapping variant regions from other studies: 53 SVs from 6 studies. See in: genome view    
Submitted genomic3,180,093-3,181,054Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4262351RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr203,199,4473,200,408
nsv4262351Submitted genomicGRCh37.p13Primary AssemblyNC_000020.10Chr203,180,0933,181,054

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15856464deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15856464RemappedPerfectNC_000020.11:g.319
9447_3200408del
GRCh38.p12First PassNC_000020.11Chr203,199,4473,200,408
nssv15856464Submitted genomicNC_000020.10:g.318
0093_3181054del
GRCh37.p13NC_000020.10Chr203,180,0933,181,054

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)
nssv158564644.6e-005121694
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