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nsv5852239

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,400

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 267 SVs from 37 studies. See in: genome view    
Submitted genomic125,096,222-125,100,621Question Mark
Overlapping variant regions from other studies: 267 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):126,108,464-126,112,863Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5852239Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8125,096,222125,100,621
nsv5852239RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8126,108,464126,112,863

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17506217copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17506217Submitted genomicGRCh38 (hg38)NC_000008.11Chr8125,096,222125,100,621
nssv17506217RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8126,108,464126,112,863

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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