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nsv5953445

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 193 SVs from 21 studies. See in: genome view    
Submitted genomic32,044,913-32,044,913Question Mark
Overlapping variant regions from other studies: 193 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):31,902,429-31,902,429Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5953445Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr832,044,91332,044,913
nsv5953445RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr831,902,42931,902,429

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17433764insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17433764Submitted genomicNC_000008.11:g.320
44913_32044914ins1
27
GRCh38 (hg38)NC_000008.11Chr832,044,91332,044,913
nssv17433764RemappedPerfectNC_000008.10:g.319
02429_31902430ins1
27
GRCh37.p13First PassNC_000008.10Chr831,902,42931,902,429

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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