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nsv5957081

  • 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: 364 SVs from 38 studies. See in: genome view    
Submitted genomic14,117,909-14,117,909Question Mark
Overlapping variant regions from other studies: 364 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):13,975,418-13,975,418Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5957081Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr814,117,90914,117,909
nsv5957081RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr813,975,41813,975,418

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17448900insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17448900Submitted genomicNC_000008.11:g.141
17909_14117910ins4
95
GRCh38 (hg38)NC_000008.11Chr814,117,90914,117,909
nssv17448900RemappedPerfectNC_000008.10:g.139
75418_13975419ins4
95
GRCh37.p13First PassNC_000008.10Chr813,975,41813,975,418

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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