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nsv5835650

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,688

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 157 SVs from 41 studies. See in: genome view    
Submitted genomic40,375,233-40,406,920Question Mark
Overlapping variant regions from other studies: 157 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):40,416,724-40,448,411Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5835650Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr340,375,23340,406,920
nsv5835650RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr340,416,72440,448,411

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17491684copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17491684Submitted genomicGRCh38 (hg38)NC_000003.12Chr340,375,23340,406,920
nssv17491684RemappedPerfectGRCh37.p13First PassNC_000003.11Chr340,416,72440,448,411

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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