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nsv1426983

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21
  • Description:MOTIF=[CGGCCC],NS=[285],REF=[3.5],RL=[21],RPA=
    [4.5],RU=[CGGCCC],QUAL=[170826]
  • Publication(s):Mallick et al. 2016

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 92 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):32,335,865-32,335,885Question Mark
Overlapping variant regions from other studies: 92 SVs from 21 studies. See in: genome view    
Submitted genomic32,801,466-32,801,486Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv1426983RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr132,335,86532,335,885
nsv1426983Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr132,801,46632,801,486

Variant Call Information

Variant Call IDTypeRepeat MotifMethodAnalysis
nssv8707398short tandem repeat(CGGCCC) 4.5SequencingGenotyping
nssv8707399short tandem repeat(CGGCCC) 3.5 (ref)SequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv8707398RemappedPerfectGRCh38.p12First PassNC_000001.11Chr132,335,86532,335,885
nssv8707399RemappedPerfectGRCh38.p12First PassNC_000001.11Chr132,335,86532,335,885
nssv8707398Submitted genomicGRCh37 (hg19)NC_000001.10Chr132,801,46632,801,486
nssv8707399Submitted genomicGRCh37 (hg19)NC_000001.10Chr132,801,46632,801,486

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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