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nsv5843693

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,850

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 165 SVs from 33 studies. See in: genome view    
Submitted genomic107,223,182-107,225,031Question Mark
Overlapping variant regions from other studies: 163 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):107,544,386-107,546,235Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5843693Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6107,223,182107,225,031
nsv5843693RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6107,544,386107,546,235

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17500880copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17500880Submitted genomicGRCh38 (hg38)NC_000006.12Chr6107,223,182107,225,031
nssv17500880RemappedPerfectGRCh37.p13First PassNC_000006.11Chr6107,544,386107,546,235

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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