U.S. flag

An official website of the United States government

nsv4559196

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,649,363

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2604 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):51,176,082-54,825,444Question Mark
Overlapping variant regions from other studies: 2607 SVs from 23 studies. See in: genome view    
Submitted genomic51,569,865-55,219,228Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4559196RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1251,176,08254,825,444
nsv4559196Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1251,569,86555,219,228

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090790inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090790RemappedPerfectNC_000012.12:g.511
76082_54825444inv
GRCh38.p12First PassNC_000012.12Chr1251,176,08254,825,444
nssv16090790Submitted genomicNC_000012.11:g.515
69865_55219228inv
GRCh37.p13NC_000012.11Chr1251,569,86555,219,228

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)
nssv160907904.6e-005121694
Support Center