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nsv6289768

  • 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: 329 SVs from 38 studies. See in: genome view    
Submitted genomic803,934-803,934Question Mark
Overlapping variant regions from other studies: 329 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):707,174-707,174Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6289768Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr17803,934803,934
nsv6289768RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr17707,174707,174

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17925824insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17925824Submitted genomicNC_000017.11:g.803
934_803935ins81
GRCh38 (hg38)NC_000017.11Chr17803,934803,934
nssv17925824RemappedPerfectNC_000017.10:g.707
174_707175ins81
GRCh37.p13First PassNC_000017.10Chr17707,174707,174

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)
nssv17925824<0.00111664
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