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nsv5974799

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,348,296

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 27636 SVs from 126 studies. See in: genome view    
Submitted genomic12,342,936-19,691,231Question Mark
Overlapping variant regions from other studies: 27638 SVs from 126 studies. See in: genome view    
Remapped(Score: Perfect):12,453,750-19,802,040Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5974799Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1912,342,93619,691,231
nsv5974799RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1912,453,75019,802,040

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17407238inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17407238Submitted genomicNC_000019.10:g.123
42936_19691231inv
GRCh38 (hg38)NC_000019.10Chr1912,342,93619,691,231
nssv17407238RemappedPerfectNC_000019.9:g.1245
3750_19802040inv
GRCh37.p13First PassNC_000019.9Chr1912,453,75019,802,040

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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