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nsv5894046

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,323

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 25 studies. See in: genome view    
Submitted genomic231,105,479-231,106,801Question Mark
Overlapping variant regions from other studies: 113 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):231,970,193-231,971,515Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5894046Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2231,105,479231,106,801
nsv5894046RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2231,970,193231,971,515

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17406134deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17406134Submitted genomicNC_000002.12:g.231
105479_231106801de
l
GRCh38 (hg38)NC_000002.12Chr2231,105,479231,106,801
nssv17406134RemappedPerfectNC_000002.11:g.231
970193_231971515de
l
GRCh37.p13First PassNC_000002.11Chr2231,970,193231,971,515

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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