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nsv5429360

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,462,166

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 8572 SVs from 111 studies. See in: genome view    
Submitted genomic111,687,835-115,150,000Question Mark
Overlapping variant regions from other studies: 8574 SVs from 111 studies. See in: genome view    
Remapped(Score: Perfect):112,230,457-115,692,621Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5429360Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1111,687,835115,150,000
nsv5429360RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1112,230,457115,692,621

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16907694duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16907694Submitted genomicNC_000001.11:g.111
687835_115150000du
p
GRCh38 (hg38)NC_000001.11Chr1111,687,835115,150,000
nssv16907694RemappedPerfectNC_000001.10:g.112
230457_115692621du
p
GRCh37.p13First PassNC_000001.10Chr1112,230,457115,692,621

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)
nssv16907694<0.00116402
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