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nsv5408126

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 32 studies. See in: genome view    
Submitted genomic158,199,217-158,199,268Question Mark
Overlapping variant regions from other studies: 106 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):158,620,249-158,620,300Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5408126Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6158,199,217158,199,268
nsv5408126RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6158,620,249158,620,300

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16990132alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16990132Submitted genomicNC_000006.12:g.158
199217_158199268in
s281
GRCh38 (hg38)NC_000006.12Chr6158,199,217158,199,268
nssv16990132RemappedPerfectNC_000006.11:g.158
620249_158620300in
s281
GRCh37.p13First PassNC_000006.11Chr6158,620,249158,620,300

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv169901320.003186404
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