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nsv5887994

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,998

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 188 SVs from 45 studies. See in: genome view    
Submitted genomic109,919,582-109,924,579Question Mark
Overlapping variant regions from other studies: 188 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):110,840,738-110,845,735Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5887994Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4109,919,582109,924,579
nsv5887994RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4110,840,738110,845,735

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17422477deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17422477Submitted genomicNC_000004.12:g.109
919582_109924579de
l
GRCh38 (hg38)NC_000004.12Chr4109,919,582109,924,579
nssv17422477RemappedPerfectNC_000004.11:g.110
840738_110845735de
l
GRCh37.p13First PassNC_000004.11Chr4110,840,738110,845,735

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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