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nsv5285145

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:930,000

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2428 SVs from 88 studies. See in: genome view    
Submitted genomic19,608,167-20,538,182Question Mark
Overlapping variant regions from other studies: 2428 SVs from 88 studies. See in: genome view    
Remapped(Score: Perfect):19,934,661-20,864,675Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5285145Submitted genomicGRCh38.p13Primary AssemblyNC_000001.11Chr119,608,177 (-10, +9)20,538,176 (-5, +6)
nsv5285145RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr119,934,671 (-10, +9)20,864,669 (-5, +6)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16739847duplicationSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16739847Submitted genomicNC_000001.11:g.(19
608167_19608186)_(
20538171_20538182)
dup
GRCh38.p13NC_000001.11Chr119,608,177 (-10, +9)20,538,176 (-5, +6)
nssv16739847RemappedPerfectNC_000001.10:g.(19
934661_19934680)_(
20864664_20864675)
dup
GRCh37.p13First PassNC_000001.10Chr119,934,671 (-10, +9)20,864,669 (-5, +6)

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)
nssv16739847<0.001
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