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nsv4566199

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,232

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 93 SVs from 9 studies. See in: genome view    
Remapped(Score: Perfect):15,419,083-15,447,314Question Mark
Overlapping variant regions from other studies: 93 SVs from 9 studies. See in: genome view    
Submitted genomic16,791,402-16,819,633Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4566199RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000021.9Chr2115,419,08315,447,314
nsv4566199Submitted genomicGRCh37.p13Primary AssemblyNC_000021.8Chr2116,791,40216,819,633

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091278inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091278RemappedPerfectNC_000021.9:g.1541
9083_15447314inv
GRCh38.p12First PassNC_000021.9Chr2115,419,08315,447,314
nssv16091278Submitted genomicNC_000021.8:g.1679
1402_16819633inv
GRCh37.p13NC_000021.8Chr2116,791,40216,819,633

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)
nssv160912784.6e-005121694
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