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nsv5205806

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:180,000

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 695 SVs from 63 studies. See in: genome view    
Submitted genomic218,240,201-218,420,200Question Mark
Overlapping variant regions from other studies: 695 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):219,104,924-219,284,923Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5205806Submitted genomicGRCh38.p13Primary AssemblyNC_000002.12Chr2218,240,201218,420,200
nsv5205806RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2219,104,924219,284,923

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16852877copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16852877Submitted genomicGRCh38.p13NC_000002.12Chr2218,240,201218,420,200
nssv16852877RemappedPerfectGRCh37.p13First PassNC_000002.11Chr2219,104,924219,284,923

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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