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nsv2215181

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22
  • Description:MOTIF=[GGGGGT],NS=[301],REF=[3.66667],RL=[22],
    RU=[GGGGGT],RPA=[3.5],QUAL=[340866]
  • Publication(s):Mallick et al. 2016

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):13,506,603-13,506,624Question Mark
Overlapping variant regions from other studies: 83 SVs from 23 studies. See in: genome view    
Submitted genomic13,548,103-13,548,124Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2215181RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr313,506,60313,506,624
nsv2215181Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr313,548,10313,548,124

Variant Call Information

Variant Call IDTypeRepeat MotifMethodAnalysis
nssv11395482short tandem repeat(GGGGGT) 3.67 (ref)SequencingGenotyping
nssv11408608short tandem repeat(GGGGGT) 3.5SequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv11395482RemappedPerfectGRCh38.p12First PassNC_000003.12Chr313,506,60313,506,624
nssv11408608RemappedPerfectGRCh38.p12First PassNC_000003.12Chr313,506,60313,506,624
nssv11395482Submitted genomicGRCh37 (hg19)NC_000003.11Chr313,548,10313,548,124
nssv11408608Submitted genomicGRCh37 (hg19)NC_000003.11Chr313,548,10313,548,124

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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