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nsv5322841

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,561

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 184 SVs from 52 studies. See in: genome view    
Submitted genomic112,292,483-112,295,043Question Mark
Overlapping variant regions from other studies: 186 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):112,835,105-112,837,665Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5322841Submitted genomicGRCh38.p13Primary AssemblyNC_000001.11Chr1112,292,483112,295,043 (-1)
nsv5322841RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1112,835,105112,837,665 (-1)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16744967sva deletionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16744967Submitted genomicNC_000001.11:g.112
292483_(112295042_
?)del
GRCh38.p13NC_000001.11Chr1112,292,483112,295,043 (-1)
nssv16744967RemappedPerfectNC_000001.10:g.112
835105_(112837664_
?)del
GRCh37.p13First PassNC_000001.10Chr1112,835,105112,837,665 (-1)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv167449670.95
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