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nsv5419869

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:48,908

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 331 SVs from 46 studies. See in: genome view    
Submitted genomic108,842,219-108,891,126Question Mark
Overlapping variant regions from other studies: 332 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):109,384,841-109,433,748Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5419869Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1108,842,219108,891,126
nsv5419869RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1109,384,841109,433,748

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16908805duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16908805Submitted genomicNC_000001.11:g.108
842219_108891126du
p
GRCh38 (hg38)NC_000001.11Chr1108,842,219108,891,126
nssv16908805RemappedPerfectNC_000001.10:g.109
384841_109433748du
p
GRCh37.p13First PassNC_000001.10Chr1109,384,841109,433,748

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)
nssv16908805<0.00126404
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