U.S. flag

An official website of the United States government

nsv5327738

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,006

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 187 SVs from 50 studies. See in: genome view    
Submitted genomic55,007,429-55,013,435Question Mark
Overlapping variant regions from other studies: 187 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):56,767,189-56,773,195Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5327738Submitted genomicGRCh38.p13Primary AssemblyNC_000010.11Chr1055,007,42955,013,434 (+1)
nsv5327738RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1056,767,18956,773,194 (+1)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16752366inversionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16752366Submitted genomicNC_000010.11:g.550
07429_(?_55013435)
inv
GRCh38.p13NC_000010.11Chr1055,007,42955,013,434 (+1)
nssv16752366RemappedPerfectNC_000010.10:g.567
67189_(?_56773195)
inv
GRCh37.p13First PassNC_000010.10Chr1056,767,18956,773,194 (+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)
nssv167523660.033
Support Center