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nsv5273757

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,700

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 30 studies. See in: genome view    
Submitted genomic110,480,201-110,484,900Question Mark
Overlapping variant regions from other studies: 96 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):110,918,006-110,922,705Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5273757Submitted genomicGRCh38.p13Primary AssemblyNC_000012.12Chr12110,480,201110,484,900
nsv5273757RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12110,918,006110,922,705

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16806854copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16806854Submitted genomicGRCh38.p13NC_000012.12Chr12110,480,201110,484,900
nssv16806854RemappedPerfectGRCh37.p13First PassNC_000012.11Chr12110,918,006110,922,705

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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