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nsv5976275

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:758,528

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2957 SVs from 104 studies. See in: genome view    
Submitted genomic10,296,446-11,054,973Question Mark
Overlapping variant regions from other studies: 2958 SVs from 104 studies. See in: genome view    
Remapped(Score: Perfect):10,449,045-11,207,572Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5976275Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1210,296,44611,054,973
nsv5976275RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,449,04511,207,572

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17367626inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17367626Submitted genomicNC_000012.12:g.102
96446_11054973inv
GRCh38 (hg38)NC_000012.12Chr1210,296,44611,054,973
nssv17367626RemappedPerfectNC_000012.11:g.104
49045_11207572inv
GRCh37.p13First PassNC_000012.11Chr1210,449,04511,207,572

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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