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nsv5925659

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:340

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 275 SVs from 56 studies. See in: genome view    
Submitted genomic86,906,418-86,906,757Question Mark
Overlapping variant regions from other studies: 275 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):88,666,175-88,666,514Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5925659Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1086,906,41886,906,757
nsv5925659RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1088,666,17588,666,514

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17352455deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17352455Submitted genomicNC_000010.11:g.869
06418_86906757del
GRCh38 (hg38)NC_000010.11Chr1086,906,41886,906,757
nssv17352455RemappedPerfectNC_000010.10:g.886
66175_88666514del
GRCh37.p13First PassNC_000010.10Chr1088,666,17588,666,514

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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