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nsv5899493

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,356

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 23 studies. See in: genome view    
Submitted genomic124,124,230-124,135,585Question Mark
Overlapping variant regions from other studies: 113 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):123,843,077-123,854,432Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5899493Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3124,124,230124,135,585
nsv5899493RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3123,843,077123,854,432

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17391016deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17391016Submitted genomicNC_000003.12:g.124
124230_124135585de
l
GRCh38 (hg38)NC_000003.12Chr3124,124,230124,135,585
nssv17391016RemappedPerfectNC_000003.11:g.123
843077_123854432de
l
GRCh37.p13First PassNC_000003.11Chr3123,843,077123,854,432

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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