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nsv5533399

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 188 SVs from 34 studies. See in: genome view    
Submitted genomic82,163,425-82,163,482Question Mark
Overlapping variant regions from other studies: 188 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):82,197,030-82,197,087Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533399Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1682,163,42582,163,482
nsv5533399RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1682,197,03082,197,087

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17709577duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17709577Submitted genomicNC_000016.10:g.821
63425_82163482dup
GRCh38 (hg38)NC_000016.10Chr1682,163,42582,163,482
nssv17709577RemappedPerfectNC_000016.9:g.8219
7030_82197087dup
GRCh37.p13First PassNC_000016.9Chr1682,197,03082,197,087

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)
nssv17709577<0.00126404
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