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nsv5087390

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 141 SVs from 25 studies. See in: genome view    
Submitted genomic193,240,915-193,240,930Question Mark
Overlapping variant regions from other studies: 141 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):192,958,704-192,958,719Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5087390Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3193,240,915193,240,930
nsv5087390RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3192,958,704192,958,719

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16623714alu insertionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16623714Submitted genomicNC_000003.12:g.193
240915_193240930in
s152
GRCh38 (hg38)NC_000003.12Chr3193,240,915193,240,930
nssv16623714RemappedPerfectNC_000003.11:g.192
958704_192958719in
s152
GRCh37.p13First PassNC_000003.11Chr3192,958,704192,958,719

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv166237140.438
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