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nsv5864050

  • 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: 114 SVs from 31 studies. See in: genome view    
Submitted genomic120,544,729-120,546,978Question Mark
Overlapping variant regions from other studies: 114 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):120,982,532-120,984,781Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5864050Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12120,544,729120,546,978
nsv5864050RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12120,982,532120,984,781

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17465828copy number variationSequencingSequence alignment2

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17465828Submitted genomicGRCh38 (hg38)NC_000012.12Chr12120,544,729120,546,978
nssv17465828RemappedPerfectGRCh37.p13First PassNC_000012.11Chr12120,982,532120,984,781

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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