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nsv5036471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,815,891

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 10444 SVs from 130 studies. See in: genome view    
Submitted genomic25,888,426-29,704,316Question Mark
Overlapping variant regions from other studies: 10459 SVs from 129 studies. See in: genome view    
Remapped(Score: Good):25,888,654-29,672,093Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5036471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr625,888,42629,704,316
nsv5036471RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr625,888,65429,672,093

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16496993inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16496993Submitted genomicNC_000006.12:g.258
88426_29704316inv
GRCh38 (hg38)NC_000006.12Chr625,888,42629,704,316
nssv16496993RemappedGoodNC_000006.11:g.258
88654_29672093inv
GRCh37.p13First PassNC_000006.11Chr625,888,65429,672,093

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16496993<0.001829246
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