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nsv5962186

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 28 studies. See in: genome view    
Submitted genomic158,169,686-158,169,686Question Mark
Overlapping variant regions from other studies: 110 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):158,590,718-158,590,718Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5962186Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6158,169,686158,169,686
nsv5962186RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6158,590,718158,590,718

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17417644insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17417644Submitted genomicNC_000006.12:g.158
169686_158169687in
s116
GRCh38 (hg38)NC_000006.12Chr6158,169,686158,169,686
nssv17417644RemappedPerfectNC_000006.11:g.158
590718_158590719in
s116
GRCh37.p13First PassNC_000006.11Chr6158,590,718158,590,718

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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