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nsv1958933

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25
  • Description:MOTIF=[TTTATT],NS=[300],REF=[4.16667],RL=[25],
    RPA=[4.33333],RU=[TTTATT],QUAL=[492514]
  • Publication(s):Mallick et al. 2016

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):39,483,847-39,483,871Question Mark
Overlapping variant regions from other studies: 114 SVs from 18 studies. See in: genome view    
Submitted genomic39,974,487-39,974,511Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv1958933RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1939,483,84739,483,871
nsv1958933Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000019.9Chr1939,974,48739,974,511

Variant Call Information

Variant Call IDTypeRepeat MotifMethodAnalysis
nssv10692560short tandem repeat(TTTATT) 4.33SequencingGenotyping
nssv10692561short tandem repeat(TTTATT) 4.17 (ref)SequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv10692560RemappedPerfectGRCh38.p12First PassNC_000019.10Chr1939,483,84739,483,871
nssv10692561RemappedPerfectGRCh38.p12First PassNC_000019.10Chr1939,483,84739,483,871
nssv10692560Submitted genomicGRCh37 (hg19)NC_000019.9Chr1939,974,48739,974,511
nssv10692561Submitted genomicGRCh37 (hg19)NC_000019.9Chr1939,974,48739,974,511

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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