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nsv5829479

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,250

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 149 SVs from 23 studies. See in: genome view    
Submitted genomic231,353,631-231,355,880Question Mark
Overlapping variant regions from other studies: 154 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):231,489,377-231,491,626Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5829479Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1231,353,631231,355,880
nsv5829479RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1231,489,377231,491,626

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17453352copy number variationSequencingSequence alignment2

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17453352Submitted genomicGRCh38 (hg38)NC_000001.11Chr1231,353,631231,355,880
nssv17453352RemappedPerfectGRCh37.p13First PassNC_000001.10Chr1231,489,377231,491,626

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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