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nsv5970558

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:103,332

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 503 SVs from 65 studies. See in: genome view    
Submitted genomic28,958,885-29,062,216Question Mark
Overlapping variant regions from other studies: 503 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):28,960,507-29,063,838Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5970558Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr428,958,88529,062,216
nsv5970558RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr428,960,50729,063,838

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17426772inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17426772Submitted genomicNC_000004.12:g.289
58885_29062216inv
GRCh38 (hg38)NC_000004.12Chr428,958,88529,062,216
nssv17426772RemappedPerfectNC_000004.11:g.289
60507_29063838inv
GRCh37.p13First PassNC_000004.11Chr428,960,50729,063,838

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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