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nsv5956827

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:274

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 128 SVs from 34 studies. See in: genome view    
Submitted genomic57,219,053-57,219,326Question Mark
Overlapping variant regions from other studies: 128 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):55,794,109-55,794,382Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5956827Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2057,219,05357,219,326
nsv5956827RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2055,794,10955,794,382

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17402088deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17402088Submitted genomicNC_000020.11:g.572
19053_57219326del
GRCh38 (hg38)NC_000020.11Chr2057,219,05357,219,326
nssv17402088RemappedPerfectNC_000020.10:g.557
94109_55794382del
GRCh37.p13First PassNC_000020.10Chr2055,794,10955,794,382

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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