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nsv5833792

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,288

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 24 studies. See in: genome view    
Submitted genomic70,171,088-70,176,375Question Mark
Overlapping variant regions from other studies: 112 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):70,398,220-70,403,507Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5833792Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr270,171,08870,176,375
nsv5833792RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr270,398,22070,403,507

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17481611copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17481611Submitted genomicGRCh38 (hg38)NC_000002.12Chr270,171,08870,176,375
nssv17481611RemappedPerfectGRCh37.p13First PassNC_000002.11Chr270,398,22070,403,507

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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