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nsv5450106

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,143

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 109 SVs from 22 studies. See in: genome view    
Submitted genomic226,776,678-226,782,820Question Mark
Overlapping variant regions from other studies: 109 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):227,641,394-227,647,536Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5450106Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2226,776,678226,782,820
nsv5450106RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2227,641,394227,647,536

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16924014duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16924014Submitted genomicNC_000002.12:g.226
776678_226782820du
p
GRCh38 (hg38)NC_000002.12Chr2226,776,678226,782,820
nssv16924014RemappedPerfectNC_000002.11:g.227
641394_227647536du
p
GRCh37.p13First PassNC_000002.11Chr2227,641,394227,647,536

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)
nssv16924014<0.00116404
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