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nsv5298537

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,176

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 118 SVs from 35 studies. See in: genome view    
Submitted genomic10,179,630-10,184,805Question Mark
Overlapping variant regions from other studies: 118 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):10,290,306-10,295,481Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5298537Submitted genomicGRCh38.p13Primary AssemblyNC_000019.10Chr1910,179,63010,184,805
nsv5298537RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1910,290,30610,295,481

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16784459copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16784459Submitted genomicGRCh38.p13NC_000019.10Chr1910,179,63010,184,805
nssv16784459RemappedPerfectGRCh37.p13First PassNC_000019.9Chr1910,290,30610,295,481

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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