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nsv5829457

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,473

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 215 SVs from 35 studies. See in: genome view    
Submitted genomic224,141,553-224,147,025Question Mark
Overlapping variant regions from other studies: 220 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):224,329,255-224,334,727Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5829457Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1224,141,553224,147,025
nsv5829457RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1224,329,255224,334,727

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17453410copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17453410Submitted genomicGRCh38 (hg38)NC_000001.11Chr1224,141,553224,147,025
nssv17453410RemappedPerfectGRCh37.p13First PassNC_000001.10Chr1224,329,255224,334,727

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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