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nsv1874232

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19
  • Description:MOTIF=[GTAG],NS=[301],REF=[4.75],RL=[19],RU=[G
    TAG],RPA=[6.75],QUAL=[187078]
  • Publication(s):Mallick et al. 2016

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):42,772,364-42,772,382Question Mark
Overlapping variant regions from other studies: 127 SVs from 16 studies. See in: genome view    
Submitted genomic40,924,382-40,924,400Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv1874232RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1742,772,36442,772,382
nsv1874232Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr1740,924,38240,924,400

Variant Call Information

Variant Call IDTypeRepeat MotifMethodAnalysis
nssv10384871short tandem repeat(GTAG) 6.75SequencingGenotyping
nssv10384872short tandem repeat(GTAG) 4.75 (ref)SequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv10384871RemappedPerfectGRCh38.p12First PassNC_000017.11Chr1742,772,36442,772,382
nssv10384872RemappedPerfectGRCh38.p12First PassNC_000017.11Chr1742,772,36442,772,382
nssv10384871Submitted genomicGRCh37 (hg19)NC_000017.10Chr1740,924,38240,924,400
nssv10384872Submitted genomicGRCh37 (hg19)NC_000017.10Chr1740,924,38240,924,400

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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